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rs606231399

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs606231399(-;-)
Make rs606231399(-;A)
Make rs606231399(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32336938
GeneBRCA2
is asnp
is mentioned by
dbSNPrs606231399
ebirs606231399
HLIrs606231399
Exacrs606231399
Varsomers606231399
Maprs606231399
PheGenIrs606231399
hapmaprs606231399
1000 genomesrs606231399
hgdprs606231399
ensemblrs606231399
gopubmedrs606231399
geneviewrs606231399
scholarrs606231399
googlers606231399
pharmgkbrs606231399
gwascentralrs606231399
openSNPrs606231399
23andMers606231399
23andMe allrs606231399
SNP Nexus

SNPshotrs606231399
SNPdbers606231399
MSV3drs606231399
GWAS Ctlgrs606231399
Max Magnitude0
ClinVar
Risk rs606231399(A;A)
Alt rs606231399(A;A)
Reference rs606231399(;)
Significance Pathogenic
Disease Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000013.10:g.32911080dupA
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000031374.7, RCV000044019.3, RCV000218358.1,