Version: 8.0.0
Date: Tue Jan 28 2025
90 results
Allele/Variant Genes: Reg4 (Rno)

(mRatBN7.2)2:185819034G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3319638234
Genes: Reg4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:185819034G>A

(mRatBN7.2)2:185821825G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3319632743
Genes: Reg4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:185821825G>A

(mRatBN7.2)2:185831689G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3319638269
Genes: Reg4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:185831689G>A

(mRatBN7.2)2:185831771C>T

(Rattus norvegicus)
Allele/Variant
Source: NC_051337.1:g.185831771C>T
Genes: Reg4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:185831771C>T

(mRatBN7.2)2:185830540G>A

(Rattus norvegicus)
Allele/Variant
Source: rs198834385
Genes: Reg4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:185830540G>A

(mRatBN7.2)2:185820374G>A

(Rattus norvegicus)
Allele/Variant
Source: rs105261135
Genes: Reg4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:185820374G>A

(mRatBN7.2)2:185821327A>C

(Rattus norvegicus)
Allele/Variant
Source: rs106305051
Genes: Reg4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:185821327A>C

(mRatBN7.2)2:185824281C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3319617677
Genes: Reg4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:185824281C>T

(mRatBN7.2)2:185824434G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3319636551
Genes: Reg4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:185824434G>A

(mRatBN7.2)2:185824671A>G

(Rattus norvegicus)
Allele/Variant
Source: rs105914791
Genes: Reg4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:185824671A>G

(mRatBN7.2)2:185831901G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3319617695
Genes: Reg4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:185831901G>A

(mRatBN7.2)2:185832203G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3319652025
Genes: Reg4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:185832203G>A

(mRatBN7.2)2:185819911C>A

(Rattus norvegicus)
Allele/Variant
Source: rs3319656962
Genes: Reg4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:185819911C>A

(mRatBN7.2)2:185830446G>A

(Rattus norvegicus)
Allele/Variant
Source: NC_051337.1:g.185830446G>A
Genes: Reg4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:185830446G>A

(mRatBN7.2)2:185821647C>T

(Rattus norvegicus)
Allele/Variant
Source: rs198766711
Genes: Reg4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:185821647C>T

(mRatBN7.2)2:185821650G>T

(Rattus norvegicus)
Allele/Variant
Source: rs105972894
Genes: Reg4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:185821650G>T

(mRatBN7.2)2:185823032A>C

(Rattus norvegicus)
Allele/Variant
Source: rs3319656934
Genes: Reg4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:185823032A>C

(mRatBN7.2)2:185825989G>C

(Rattus norvegicus)
Allele/Variant
Source: rs3319640173
Genes: Reg4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:185825989G>C

(mRatBN7.2)2:185832232C>T

(Rattus norvegicus)
Allele/Variant
Source: rs199173145
Genes: Reg4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:185832232C>T

(mRatBN7.2)2:185826383A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3319645824
Genes: Reg4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:185826383A>G

(mRatBN7.2)2:185832977G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3319651267
Genes: Reg4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:185832977G>A

(mRatBN7.2)2:185831438C>T

(Rattus norvegicus)
Allele/Variant
Source: rs105690892
Genes: Reg4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:185831438C>T

(mRatBN7.2)2:185825869G>C

(Rattus norvegicus)
Allele/Variant
Source: rs3319640124
Genes: Reg4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:185825869G>C

(mRatBN7.2)2:185833102G>T

(Rattus norvegicus)
Allele/Variant
Source: rs3319632697
Genes: Reg4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:185833102G>T

(mRatBN7.2)2:185825724G>C

(Rattus norvegicus)
Allele/Variant
Source: NC_051337.1:g.185825724G>C
Genes: Reg4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:185825724G>C

(mRatBN7.2)2:185833034G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3319651257
Genes: Reg4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:185833034G>A

(mRatBN7.2)2:185826019T>A

(Rattus norvegicus)
Allele/Variant
Source: rs3319640070
Genes: Reg4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:185826019T>A

(mRatBN7.2)2:185825714C>G

(Rattus norvegicus)
Allele/Variant
Source: NC_051337.1:g.185825714C>G
Genes: Reg4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:185825714C>G

(mRatBN7.2)2:185829312G>A

(Rattus norvegicus)
Allele/Variant
Source: NC_051337.1:g.185829312G>A
Genes: Reg4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:185829312G>A

(mRatBN7.2)2:185830708G>T

(Rattus norvegicus)
Allele/Variant
Source: rs105263605
Genes: Reg4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:185830708G>T

(mRatBN7.2)2:185824997G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3319616336
Genes: Reg4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:185824997G>A

(mRatBN7.2)2:185831834T>C

(Rattus norvegicus)
Allele/Variant
Source: rs106697374
Genes: Reg4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:185831834T>C

(mRatBN7.2)2:185832884A>G

(Rattus norvegicus)
Allele/Variant
Source: rs107518179
Genes: Reg4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:185832884A>G

(mRatBN7.2)2:185827760T>G

(Rattus norvegicus)
Allele/Variant
Source: rs3319645888
Genes: Reg4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:185827760T>G

(mRatBN7.2)2:185830475T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3319646825
Genes: Reg4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:185830475T>C

(mRatBN7.2)2:185827273T>G

(Rattus norvegicus)
Allele/Variant
Source: rs105041623
Genes: Reg4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:185827273T>G

(mRatBN7.2)2:185821567T>A

(Rattus norvegicus)
Allele/Variant
Source: rs3319651255
Genes: Reg4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:185821567T>A

(mRatBN7.2)2:185822647G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3319601706
Genes: Reg4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:185822647G>A

(mRatBN7.2)2:185833109C>T

(Rattus norvegicus)
Allele/Variant
Source: rs8158227
Genes: Reg4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:185833109C>T

(mRatBN7.2)2:185826958A>G

(Rattus norvegicus)
Allele/Variant
Source: rs106599784
Genes: Reg4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:185826958A>G

(mRatBN7.2)2:185826359A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3319601716
Genes: Reg4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:185826359A>G

(mRatBN7.2)2:185828112A>G

(Rattus norvegicus)
Allele/Variant
Source: rs107190202
Genes: Reg4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:185828112A>G

(mRatBN7.2)2:185826930T>C

(Rattus norvegicus)
Allele/Variant
Source: rs106860626
Genes: Reg4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:185826930T>C

(mRatBN7.2)2:185829221G>T

(Rattus norvegicus)
Allele/Variant
Source: rs105144379
Genes: Reg4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:185829221G>T

(mRatBN7.2)2:185820039C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3319569397
Genes: Reg4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:185820039C>T

(mRatBN7.2)2:185821352C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3319640115
Genes: Reg4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:185821352C>T

(mRatBN7.2)2:185826423C>T

(Rattus norvegicus)
Allele/Variant
Source: rs107032737
Genes: Reg4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:185826423C>T

(mRatBN7.2)2:185831026T>G

(Rattus norvegicus)
Allele/Variant
Source: rs105782039
Genes: Reg4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:185831026T>G

(mRatBN7.2)2:185825480C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3319636576
Genes: Reg4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:185825480C>T

(mRatBN7.2)2:185826013G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3319656963
Genes: Reg4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:185826013G>A