rs161927
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs161927(A;A) |
Make rs161927(A;G) |
Make rs161927(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 7796555 |
is a | snp |
is | mentioned by |
dbSNP | rs161927 |
dbSNP (classic) | rs161927 |
ClinGen | rs161927 |
ebi | rs161927 |
HLI | rs161927 |
Exac | rs161927 |
Gnomad | rs161927 |
Varsome | rs161927 |
LitVar | rs161927 |
Map | rs161927 |
PheGenI | rs161927 |
Biobank | rs161927 |
1000 genomes | rs161927 |
hgdp | rs161927 |
ensembl | rs161927 |
geneview | rs161927 |
scholar | rs161927 |
rs161927 | |
pharmgkb | rs161927 |
gwascentral | rs161927 |
openSNP | rs161927 |
23andMe | rs161927 |
SNPshot | rs161927 |
SNPdbe | rs161927 |
MSV3d | rs161927 |
GWAS Ctlg | rs161927 |
GMAF | 0.1598 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 20068591] A genome-wide association study for age-related hearing impairment in the Saami