Have questions? Visit https://www.reddit.com/r/SNPedia

rs62543585

From SNPedia

Orientationplus
Make rs62543585(C;C)
Make rs62543585(C;T)
Make rs62543585(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome9
Position16906891
is asnp
is mentioned by
dbSNPrs62543585
ebirs62543585
HLIrs62543585
Exacrs62543585
Varsomers62543585
Maprs62543585
PheGenIrs62543585
hapmaprs62543585
1000 genomesrs62543585
hgdprs62543585
ensemblrs62543585
gopubmedrs62543585
geneviewrs62543585
scholarrs62543585
googlers62543585
pharmgkbrs62543585
gwascentralrs62543585
openSNPrs62543585
23andMers62543585
23andMe allrs62543585
SNP Nexus

SNPshotrs62543585
SNPdbers62543585
MSV3drs62543585
GWAS Ctlgrs62543585
Max Magnitude

[PMID 27463617] Fine-Scale Mapping at 9p22.2 Identifies Candidate Causal Variants That Modify Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers.