rs11895168
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11895168(A;A) |
Make rs11895168(A;C) |
Make rs11895168(C;C) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 2 |
Position | 211377467 |
Gene | ERBB4 |
is a | snp |
is | mentioned by |
dbSNP | rs11895168 |
dbSNP (classic) | rs11895168 |
ClinGen | rs11895168 |
ebi | rs11895168 |
HLI | rs11895168 |
Exac | rs11895168 |
Gnomad | rs11895168 |
Varsome | rs11895168 |
LitVar | rs11895168 |
Map | rs11895168 |
PheGenI | rs11895168 |
Biobank | rs11895168 |
1000 genomes | rs11895168 |
hgdp | rs11895168 |
ensembl | rs11895168 |
geneview | rs11895168 |
scholar | rs11895168 |
rs11895168 | |
pharmgkb | rs11895168 |
gwascentral | rs11895168 |
openSNP | rs11895168 |
23andMe | rs11895168 |
SNPshot | rs11895168 |
SNPdbe | rs11895168 |
MSV3d | rs11895168 |
GWAS Ctlg | rs11895168 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 27262100] rs11895168 C allele and the increased risk of breast cancer in Isfahan population.