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rs587781629

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587781629(A;A)
Make rs587781629(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32333388
GeneBRCA2
is asnp
is mentioned by
dbSNPrs587781629
ebirs587781629
HLIrs587781629
Exacrs587781629
Varsomers587781629
Maprs587781629
PheGenIrs587781629
hapmaprs587781629
1000 genomesrs587781629
hgdprs587781629
ensemblrs587781629
gopubmedrs587781629
geneviewrs587781629
scholarrs587781629
googlers587781629
pharmgkbrs587781629
gwascentralrs587781629
openSNPrs587781629
23andMers587781629
23andMe allrs587781629
SNP Nexus

SNPshotrs587781629
SNPdbers587781629
MSV3drs587781629
GWAS Ctlgrs587781629
Max Magnitude0
ClinVar
Risk rs587781629(A;A)
Alt rs587781629(A;A)
Reference rs587781629(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome not provided Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 1 Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32907525G>A
CLNSRC
CLNACC RCV000129734.2, RCV000160183.2, RCV000204822.1, RCV000210109.1, RCV000238861.1,