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rs10124837

From SNPedia

Orientationplus
Make rs10124837(C;C)
Make rs10124837(C;T)
Make rs10124837(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome9
Position16891649
is asnp
is mentioned by
dbSNPrs10124837
ebirs10124837
HLIrs10124837
Exacrs10124837
Varsomers10124837
Maprs10124837
PheGenIrs10124837
hapmaprs10124837
1000 genomesrs10124837
hgdprs10124837
ensemblrs10124837
gopubmedrs10124837
geneviewrs10124837
scholarrs10124837
googlers10124837
pharmgkbrs10124837
gwascentralrs10124837
openSNPrs10124837
23andMers10124837
23andMe allrs10124837
SNP Nexus

SNPshotrs10124837
SNPdbers10124837
MSV3drs10124837
GWAS Ctlgrs10124837
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.