rs267606631
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs267606631(A;A) |
Make rs267606631(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 81511269 |
Gene | ACTG1, FSCN2 |
is a | snp |
is | mentioned by |
dbSNP | rs267606631 |
dbSNP (classic) | rs267606631 |
ClinGen | rs267606631 |
ebi | rs267606631 |
HLI | rs267606631 |
Exac | rs267606631 |
Gnomad | rs267606631 |
Varsome | rs267606631 |
LitVar | rs267606631 |
Map | rs267606631 |
PheGenI | rs267606631 |
Biobank | rs267606631 |
1000 genomes | rs267606631 |
hgdp | rs267606631 |
ensembl | rs267606631 |
geneview | rs267606631 |
scholar | rs267606631 |
rs267606631 | |
pharmgkb | rs267606631 |
gwascentral | rs267606631 |
openSNP | rs267606631 |
23andMe | rs267606631 |
SNPshot | rs267606631 |
SNPdbe | rs267606631 |
MSV3d | rs267606631 |
GWAS Ctlg | rs267606631 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs267606631(A;A) |
Alt | rs267606631(A;A) |
Reference | Rs267606631(G;G) |
Significance | Pathogenic |
Disease | Deafness not provided Nonsyndromic hearing loss and deafness |
Variation | info |
Gene | ACTG1 |
CLNDBN | Deafness, autosomal dominant 20 not provided Nonsyndromic hearing loss and deafness |
Reversed | 1 |
HGVS | NC_000017.10:g.79478295C>T |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) UniProtKB (variants) |
CLNACC | RCV000019987.30, RCV000059728.1, RCV000211710.1, |
[PMID 19477959] In vivo and in vitro effects of two novel gamma-actin (ACTG1) mutations that cause DFNA20/26 hearing impairment.