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rs397507603

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397507603(G;T)
Make rs397507603(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32319181
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507603
ebirs397507603
HLIrs397507603
Exacrs397507603
Varsomers397507603
Maprs397507603
PheGenIrs397507603
hapmaprs397507603
1000 genomesrs397507603
hgdprs397507603
ensemblrs397507603
gopubmedrs397507603
geneviewrs397507603
scholarrs397507603
googlers397507603
pharmgkbrs397507603
gwascentralrs397507603
openSNPrs397507603
23andMers397507603
23andMe allrs397507603
SNP Nexus

SNPshotrs397507603
SNPdbers397507603
MSV3drs397507603
GWAS Ctlgrs397507603
Max Magnitude0
ClinVar
Risk rs397507603(A,T;A,T)
Alt rs397507603(A,T;A,T)
Reference rs397507603(G;G)
Significance Untested
Disease Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome Tumor susceptibility linked to germline BAP1 mutations Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome Tumor susceptibility linked to germline BAP1 mutations Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32893318G>A; NC_000013.10:g.32893318G>T
CLNSRC ClinVar
CLNACC RCV000077663.2, RCV000195636.1, RCV000216277.1, RCV000043868.2,