Version: 8.0.0
Date: Tue Jan 28 2025
11 results
Allele/Variant Genes: LRATD1 (Hsa)

(GRCh38)2:14634484G>A

(Homo sapiens)
Allele/Variant
Source: rs751370026
Genes: LRATD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:14634484G>A

(GRCh38)2:14634723C>G

(Homo sapiens)
Allele/Variant
Source: rs367691817
Genes: LRATD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:14634723C>G

(GRCh38)2:14634847G>T

(Homo sapiens)
Allele/Variant
Source: rs544194083
Genes: LRATD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:14634847G>T

(GRCh38)2:14634060C>G

(Homo sapiens)
Allele/Variant
Source: rs750822633
Genes: LRATD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:14634060C>G

(GRCh38)2:14634389C>T

(Homo sapiens)
Allele/Variant
Source: rs991310610
Genes: LRATD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:14634389C>T

(GRCh38)2:14634155C>T

(Homo sapiens)
Allele/Variant
Source: rs1296804230
Genes: LRATD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:14634155C>T

(GRCh38)2:14634494C>G

(Homo sapiens)
Allele/Variant
Source: rs752734357
Genes: LRATD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:14634494C>G

(GRCh38)2:14634592G>C

(Homo sapiens)
Allele/Variant
Source: rs779300890
Genes: LRATD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:14634592G>C

(GRCh38)2:14634788G>A

(Homo sapiens)
Allele/Variant
Source: rs145966184
Genes: LRATD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:14634788G>A

(GRCh38)2:14634099T>G

(Homo sapiens)
Allele/Variant
Source: rs770803343
Genes: LRATD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:14634099T>G

(GRCh38)2:14634080C>G

(Homo sapiens)
Allele/Variant
Source: rs1013264110
Genes: LRATD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:14634080C>G