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rs397507671

From SNPedia

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


Make rs397507671(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32337820
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507671
ClinGenrs397507671
ebirs397507671
HLIrs397507671
Exacrs397507671
Varsomers397507671
Maprs397507671
PheGenIrs397507671
hapmaprs397507671
1000 genomesrs397507671
hgdprs397507671
ensemblrs397507671
gopubmedrs397507671
geneviewrs397507671
scholarrs397507671
googlers397507671
pharmgkbrs397507671
gwascentralrs397507671
openSNPrs397507671
23andMers397507671
23andMe allrs397507671
SNP Nexus

SNPshotrs397507671
SNPdbers397507671
MSV3drs397507671
GWAS Ctlgrs397507671
Max Magnitude6
ClinVar
Risk rs397507671(-;-)
Alt rs397507671(-;-)
Reference Rs397507671(TT;TT)
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.32911957_32911958delTT
CLNSRC ClinVar
CLNACC RCV000044203.2, RCV000241218.2,