rs12984523
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12984523(C;C) |
Make rs12984523(C;T) |
Make rs12984523(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 19 |
Position | 10196143 |
Gene | DNMT1 |
is a | snp |
is | mentioned by |
dbSNP | rs12984523 |
dbSNP (classic) | rs12984523 |
ClinGen | rs12984523 |
ebi | rs12984523 |
HLI | rs12984523 |
Exac | rs12984523 |
Gnomad | rs12984523 |
Varsome | rs12984523 |
LitVar | rs12984523 |
Map | rs12984523 |
PheGenI | rs12984523 |
Biobank | rs12984523 |
1000 genomes | rs12984523 |
hgdp | rs12984523 |
ensembl | rs12984523 |
geneview | rs12984523 |
scholar | rs12984523 |
rs12984523 | |
pharmgkb | rs12984523 |
gwascentral | rs12984523 |
openSNP | rs12984523 |
23andMe | rs12984523 |
SNPshot | rs12984523 |
SNPdbe | rs12984523 |
MSV3d | rs12984523 |
GWAS Ctlg | rs12984523 |
GMAF | 0.4564 |
Max Magnitude | 0 |
[PMID 23771421] Lack of association between DNMT1 gene polymorphisms and noise-induced hearing loss in a Chinese population
[PMID 24630008] [Association between SNPs in DNMT1 and noise-induced hearing loss in Chinese Han population]