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rs730881573

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730881573(C;C)
Make rs730881573(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32397045
GeneBRCA2
is asnp
is mentioned by
dbSNPrs730881573
ebirs730881573
HLIrs730881573
Exacrs730881573
Varsomers730881573
Maprs730881573
PheGenIrs730881573
hapmaprs730881573
1000 genomesrs730881573
hgdprs730881573
ensemblrs730881573
gopubmedrs730881573
geneviewrs730881573
scholarrs730881573
googlers730881573
pharmgkbrs730881573
gwascentralrs730881573
openSNPrs730881573
23andMers730881573
23andMe allrs730881573
SNP Nexus

SNPshotrs730881573
SNPdbers730881573
MSV3drs730881573
GWAS Ctlgrs730881573
Max Magnitude0
ClinVar
Risk rs730881573(C;C)
Alt rs730881573(C;C)
Reference rs730881573(G;G)
Significance Pathogenic
Disease not provided Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN not provided Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32971182G>C
CLNSRC
CLNACC RCV000160176.1, RCV000239346.1,