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rs730881581

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;G) 6 BRCA2 variant considered pathogenic for breast cancer
(G;G) 0 common in clinvar


Make rs730881581(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32363376
GeneBRCA2
is asnp
is mentioned by
dbSNPrs730881581
dbSNP (old)rs730881581
ClinGenrs730881581
ebirs730881581
HLIrs730881581
Exacrs730881581
Gnomadrs730881581
Varsomers730881581
Maprs730881581
PheGenIrs730881581
Biobankrs730881581
1000 genomesrs730881581
hgdprs730881581
ensemblrs730881581
gopubmedrs730881581
geneviewrs730881581
scholarrs730881581
googlers730881581
pharmgkbrs730881581
gwascentralrs730881581
openSNPrs730881581
23andMers730881581
23andMe allrs730881581
SNP Nexus

SNPshotrs730881581
SNPdbers730881581
MSV3drs730881581
GWAS Ctlgrs730881581
Max Magnitude6
ClinVar
Risk rs730881581(A;A)
Alt rs730881581(A;A)
Reference Rs730881581(G;G)
Significance Pathogenic
Disease not provided Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA2
CLNDBN not provided Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000013.10:g.32937513G>A
CLNSRC
CLNACC RCV000160191.2, RCV000241299.2, RCV000460183.1,