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rs397507865

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CATT;CATT) 0 common in clinvar
(TCAT;TCAT) 0 common in clinvar
Make rs397507865(-;-)
Make rs397507865(-;TCAT)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340886
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507865
ebirs397507865
HLIrs397507865
Exacrs397507865
Varsomers397507865
Maprs397507865
PheGenIrs397507865
hapmaprs397507865
1000 genomesrs397507865
hgdprs397507865
ensemblrs397507865
gopubmedrs397507865
geneviewrs397507865
scholarrs397507865
googlers397507865
pharmgkbrs397507865
gwascentralrs397507865
openSNPrs397507865
23andMers397507865
23andMe allrs397507865
SNP Nexus

SNPshotrs397507865
SNPdbers397507865
MSV3drs397507865
GWAS Ctlgrs397507865
Max Magnitude0
ClinVar
Risk rs397507865(;)
Alt rs397507865(;)
Reference rs397507865(CATT;CATT)
Significance Pathogenic
Disease Familial cancer of breast Tumor susceptibility linked to germline BAP1 mutations Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Tumor susceptibility linked to germline BAP1 mutations Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000013.10:g.32915023_32915026delTCAT
CLNSRC ClinVar
CLNACC RCV000044977.4, RCV000221260.1, RCV000225746.1,