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rs606231396

From SNPedia

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Geno Mag Summary
(;) 0 common in clinvar
Make rs606231396(-;-)
Make rs606231396(-;G)
Make rs606231396(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32333020
GeneBRCA2
is asnp
is mentioned by
dbSNPrs606231396
ebirs606231396
HLIrs606231396
Exacrs606231396
Varsomers606231396
Maprs606231396
PheGenIrs606231396
hapmaprs606231396
1000 genomesrs606231396
hgdprs606231396
ensemblrs606231396
gopubmedrs606231396
geneviewrs606231396
scholarrs606231396
googlers606231396
pharmgkbrs606231396
gwascentralrs606231396
openSNPrs606231396
23andMers606231396
23andMe allrs606231396
SNP Nexus

SNPshotrs606231396
SNPdbers606231396
MSV3drs606231396
GWAS Ctlgrs606231396
Max Magnitude0
ClinVar
Risk rs606231396(G;G)
Alt rs606231396(G;G)
Reference rs606231396(;)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32907157dupG
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000112932.1,