rs11928865
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common/normal |
Make rs11928865(A;A) |
Make rs11928865(A;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 7114015 |
Gene | GRM7 |
is a | snp |
is | mentioned by |
dbSNP | rs11928865 |
dbSNP (classic) | rs11928865 |
ClinGen | rs11928865 |
ebi | rs11928865 |
HLI | rs11928865 |
Exac | rs11928865 |
Gnomad | rs11928865 |
Varsome | rs11928865 |
LitVar | rs11928865 |
Map | rs11928865 |
PheGenI | rs11928865 |
Biobank | rs11928865 |
1000 genomes | rs11928865 |
hgdp | rs11928865 |
ensembl | rs11928865 |
geneview | rs11928865 |
scholar | rs11928865 |
rs11928865 | |
pharmgkb | rs11928865 |
gwascentral | rs11928865 |
openSNP | rs11928865 |
23andMe | rs11928865 |
SNPshot | rs11928865 |
SNPdbe | rs11928865 |
MSV3d | rs11928865 |
GWAS Ctlg | rs11928865 |
Max Magnitude | 0 |
? | (A;A) (A;T) (T;T) | 28 |
---|---|---|
|
[PMID 24146964] Association of GRM7 variants with different phenotype patterns of age-related hearing impairment in an elderly male Han Chinese population