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rs587776351

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587776351(A;A)
Make rs587776351(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32370958
GeneBRCA2
is asnp
is mentioned by
dbSNPrs587776351
ebirs587776351
HLIrs587776351
Exacrs587776351
Varsomers587776351
Maprs587776351
PheGenIrs587776351
hapmaprs587776351
1000 genomesrs587776351
hgdprs587776351
ensemblrs587776351
gopubmedrs587776351
geneviewrs587776351
scholarrs587776351
googlers587776351
pharmgkbrs587776351
gwascentralrs587776351
openSNPrs587776351
23andMers587776351
23andMe allrs587776351
SNP Nexus

SNPshotrs587776351
SNPdbers587776351
MSV3drs587776351
GWAS Ctlgrs587776351
Max Magnitude0
ClinVar
Risk rs587776351(A;A)
Alt rs587776351(A;A)
Reference rs587776351(G;G)
Significance Pathogenic
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32945095G>A
CLNSRC
CLNACC RCV000143787.1,