rs74315438
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 6 | Deafness; early-onset (prelingual) |
(A;G) | 3 | Carrier of a deafness mutation |
(G;G) | 0 | common in clinvar |
Reference | GRCh38 38.1/141 |
Chromosome | 21 |
Position | 36461395 |
Gene | CLDN14, LOC105369301 |
is a | snp |
is | mentioned by |
dbSNP | rs74315438 |
dbSNP (classic) | rs74315438 |
ClinGen | rs74315438 |
ebi | rs74315438 |
HLI | rs74315438 |
Exac | rs74315438 |
Gnomad | rs74315438 |
Varsome | rs74315438 |
LitVar | rs74315438 |
Map | rs74315438 |
PheGenI | rs74315438 |
Biobank | rs74315438 |
1000 genomes | rs74315438 |
hgdp | rs74315438 |
ensembl | rs74315438 |
geneview | rs74315438 |
scholar | rs74315438 |
rs74315438 | |
pharmgkb | rs74315438 |
gwascentral | rs74315438 |
openSNP | rs74315438 |
23andMe | rs74315438 |
SNPshot | rs74315438 |
SNPdbe | rs74315438 |
MSV3d | rs74315438 |
GWAS Ctlg | rs74315438 |
Max Magnitude | 6 |
rs74315438, also known as c.301G>A, p.Gly101Arg and G101R, represents a variant in the CLDN14 gene on chromosome 21.
Inherited in a recessive manner, the minor allele of this SNP is considered pathogenic for a form of deafness; see OMIM and ClinVar sidebars for details.
ClinVar | |
---|---|
Risk | Rs74315438(A;A) |
Alt | Rs74315438(A;A) |
Reference | Rs74315438(G;G) |
Significance | Pathogenic |
Disease | Deafness |
Variation | info |
Gene | CLDN14 |
CLNDBN | Deafness, autosomal recessive 29 |
Reversed | 1 |
HGVS | NC_000021.8:g.37833693C>T |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000005125.3, |