Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: RXRA (Hsa)
(GRCh38)9:134417195C>A
(Homo sapiens)Allele/Variant
Source: rs146295223
Genes: RXRA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:134417195C>A
(GRCh38)9:134417178C>T
(Homo sapiens)Allele/Variant
Source: rs1348109062
Genes: RXRA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:134417178C>T
(GRCh38)9:134436505C>A
(Homo sapiens)Allele/Variant
Source: rs1057519958
Genes: RXRA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:134436505C>A
(GRCh38)9:134436587G>A
(Homo sapiens)Allele/Variant
Source: rs1390461687
Genes: RXRA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:134436587G>A
(GRCh38)9:134409102T>C
(Homo sapiens)Allele/Variant
Source: rs778077188
Genes: RXRA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:134409102T>C
(GRCh38)9:134401735G>A
(Homo sapiens)Allele/Variant
Source: rs200082299
Genes: RXRA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:134401735G>A
(GRCh38)9:134434138C>T
(Homo sapiens)Allele/Variant
Source: rs753474465
Genes: RXRA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:134434138C>T
(GRCh38)9:134417221G>A
(Homo sapiens)Allele/Variant
Source: rs781281765
Genes: RXRA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:134417221G>A
(GRCh38)9:134436600C>T
(Homo sapiens)Allele/Variant
Source: NC_000009.12:g.134436600C>T
Genes: RXRA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:134436600C>T
(GRCh38)9:134436594G>A
(Homo sapiens)Allele/Variant
Source: rs1468244890
Genes: RXRA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:134436594G>A
(GRCh38)9:134417311G>C
(Homo sapiens)Allele/Variant
Source: rs986185258
Genes: RXRA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:134417311G>C
(GRCh38)9:134417208G>C
(Homo sapiens)Allele/Variant
Source: NC_000009.12:g.134417208G>C
Genes: RXRA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:134417208G>C
(GRCh38)9:134417218G>A
(Homo sapiens)Allele/Variant
Source: rs1588299621
Genes: RXRA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:134417218G>A
(GRCh38)9:134436505C>T
(Homo sapiens)Allele/Variant
Source: rs1057519958
Genes: RXRA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:134436505C>T
(GRCh38)9:134326660G>A
(Homo sapiens)Allele/Variant
Source: rs1834915264
Genes: RXRA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, splice_donor_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:134326660G>A
(GRCh38)9:134436595C>T
(Homo sapiens)Allele/Variant
Source: rs1306245171
Genes: RXRA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:134436595C>T
(GRCh38)9:134409080C>T
(Homo sapiens)Allele/Variant
Source: rs748518062
Genes: RXRA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:134409080C>T
(GRCh38)9:134319017T>C
(Homo sapiens)Allele/Variant
Source: rs11185644
Genes: RXRA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:134319017T>C
(GRCh38)9:134401726C>T
(Homo sapiens)Allele/Variant
Source: rs1805337
Genes: RXRA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:134401726C>T