rs3735713
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs3735713(A;A) |
Make rs3735713(A;G) |
Make rs3735713(G;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 8 |
Position | 101666744 |
Gene | GRHL2 |
is a | snp |
is | mentioned by |
dbSNP | rs3735713 |
dbSNP (classic) | rs3735713 |
ClinGen | rs3735713 |
ebi | rs3735713 |
HLI | rs3735713 |
Exac | rs3735713 |
Gnomad | rs3735713 |
Varsome | rs3735713 |
LitVar | rs3735713 |
Map | rs3735713 |
PheGenI | rs3735713 |
Biobank | rs3735713 |
1000 genomes | rs3735713 |
hgdp | rs3735713 |
ensembl | rs3735713 |
geneview | rs3735713 |
scholar | rs3735713 |
rs3735713 | |
pharmgkb | rs3735713 |
gwascentral | rs3735713 |
openSNP | rs3735713 |
23andMe | rs3735713 |
SNPshot | rs3735713 |
SNPdbe | rs3735713 |
MSV3d | rs3735713 |
GWAS Ctlg | rs3735713 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 27318899] [Association between grainyhead-like 2 gene polymorphisms and noise-induced hearing loss].