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rs11895168

From SNPedia

Orientationplus
Make rs11895168(A;A)
Make rs11895168(A;C)
Make rs11895168(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position211377467
GeneERBB4
is asnp
is mentioned by
dbSNPrs11895168
ebirs11895168
HLIrs11895168
Exacrs11895168
Varsomers11895168
Maprs11895168
PheGenIrs11895168
hapmaprs11895168
1000 genomesrs11895168
hgdprs11895168
ensemblrs11895168
gopubmedrs11895168
geneviewrs11895168
scholarrs11895168
googlers11895168
pharmgkbrs11895168
gwascentralrs11895168
openSNPrs11895168
23andMers11895168
23andMe allrs11895168
SNP Nexus

SNPshotrs11895168
SNPdbers11895168
MSV3drs11895168
GWAS Ctlgrs11895168
Max Magnitude
? (A;A) (A;C) (C;C) 28

[PMID 27262100] rs11895168 C allele and the increased risk of breast cancer in Isfahan population.