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rs587782612

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587782612(A;A)
Make rs587782612(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32396957
GeneBRCA2
is asnp
is mentioned by
dbSNPrs587782612
ebirs587782612
HLIrs587782612
Exacrs587782612
Varsomers587782612
Maprs587782612
PheGenIrs587782612
hapmaprs587782612
1000 genomesrs587782612
hgdprs587782612
ensemblrs587782612
gopubmedrs587782612
geneviewrs587782612
scholarrs587782612
googlers587782612
pharmgkbrs587782612
gwascentralrs587782612
openSNPrs587782612
23andMers587782612
23andMe allrs587782612
SNP Nexus

SNPshotrs587782612
SNPdbers587782612
MSV3drs587782612
GWAS Ctlgrs587782612
Max Magnitude0
ClinVar
Risk rs587782612(A;A)
Alt rs587782612(A;A)
Reference rs587782612(T;T)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32971094T>A
CLNSRC
CLNACC RCV000131987.2,