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rs606231403

From SNPedia

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Geno Mag Summary
(;) 0 common in clinvar
Make rs606231403(-;-)
Make rs606231403(-;T)
Make rs606231403(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32340286
GeneBRCA2
is asnp
is mentioned by
dbSNPrs606231403
ebirs606231403
HLIrs606231403
Exacrs606231403
Varsomers606231403
Maprs606231403
PheGenIrs606231403
hapmaprs606231403
1000 genomesrs606231403
hgdprs606231403
ensemblrs606231403
gopubmedrs606231403
geneviewrs606231403
scholarrs606231403
googlers606231403
pharmgkbrs606231403
gwascentralrs606231403
openSNPrs606231403
23andMers606231403
23andMe allrs606231403
SNP Nexus

SNPshotrs606231403
SNPdbers606231403
MSV3drs606231403
GWAS Ctlgrs606231403
Max Magnitude0
ClinVar
Risk rs606231403(T;T)
Alt rs606231403(T;T)
Reference rs606231403(;)
Significance Pathogenic
Disease Breast-ovarian cancer Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32914426dupT
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000113505.1, RCV000164167.1,