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rs397507768

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397507768(G;T)
Make rs397507768(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32326499
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507768
ebirs397507768
HLIrs397507768
Exacrs397507768
Varsomers397507768
Maprs397507768
PheGenIrs397507768
hapmaprs397507768
1000 genomesrs397507768
hgdprs397507768
ensemblrs397507768
gopubmedrs397507768
geneviewrs397507768
scholarrs397507768
googlers397507768
pharmgkbrs397507768
gwascentralrs397507768
openSNPrs397507768
23andMers397507768
23andMe allrs397507768
SNP Nexus

SNPshotrs397507768
SNPdbers397507768
MSV3drs397507768
GWAS Ctlgrs397507768
Max Magnitude0
ClinVar
Risk rs397507768(C,T;C,T)
Alt rs397507768(C,T;C,T)
Reference rs397507768(G;G)
Significance Untested
Disease not specified Tumor susceptibility linked to germline BAP1 mutations Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN not specified Tumor susceptibility linked to germline BAP1 mutations Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32900636G>C; NC_000013.10:g.32900636G>T
CLNSRC ClinVar
CLNACC RCV000168537.2, RCV000222599.1, RCV000044593.2, RCV000220016.1, RCV000239003.1,