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rs397508012

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs397508012(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32379383
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508012
dbSNP (old)rs397508012
ClinGenrs397508012
ebirs397508012
HLIrs397508012
Exacrs397508012
Varsomers397508012
Maprs397508012
PheGenIrs397508012
Biobankrs397508012
1000 genomesrs397508012
hgdprs397508012
ensemblrs397508012
gopubmedrs397508012
geneviewrs397508012
scholarrs397508012
googlers397508012
pharmgkbrs397508012
gwascentralrs397508012
openSNPrs397508012
23andMers397508012
23andMe allrs397508012
SNP Nexus

SNPshotrs397508012
SNPdbers397508012
MSV3drs397508012
GWAS Ctlgrs397508012
Max Magnitude6
ClinVar
Risk rs397508012(T;T)
Alt rs397508012(T;T)
Reference Rs397508012(C;C)
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.32953520C>T
CLNSRC ClinVar
CLNACC RCV000045635.2, RCV000256787.2,