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rs397507723

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;G) 6 BRCA2 variant considered pathogenic for breast cancer
(G;G) 0 common in clinvar


Make rs397507723(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32338890
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507723
dbSNP (classic)rs397507723
ClinGenrs397507723
ebirs397507723
HLIrs397507723
Exacrs397507723
Gnomadrs397507723
Varsomers397507723
LitVarrs397507723
Maprs397507723
PheGenIrs397507723
Biobankrs397507723
1000 genomesrs397507723
hgdprs397507723
ensemblrs397507723
geneviewrs397507723
scholarrs397507723
googlers397507723
pharmgkbrs397507723
gwascentralrs397507723
openSNPrs397507723
23andMers397507723
SNPshotrs397507723
SNPdbers397507723
MSV3drs397507723
GWAS Ctlgrs397507723
Max Magnitude6
ClinVar
Risk rs397507723(-;-)
Alt rs397507723(-;-)
Reference Rs397507723(G;G)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32913027delG
CLNSRC ClinVar
CLNACC RCV000044430.2, RCV000240992.2,