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rs397507334

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
(-;A) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs397507334(A;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32338825
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507334
dbSNP (old)rs397507334
ClinGenrs397507334
ebirs397507334
HLIrs397507334
Exacrs397507334
Varsomers397507334
Maprs397507334
PheGenIrs397507334
Biobankrs397507334
1000 genomesrs397507334
hgdprs397507334
ensemblrs397507334
gopubmedrs397507334
geneviewrs397507334
scholarrs397507334
googlers397507334
pharmgkbrs397507334
gwascentralrs397507334
openSNPrs397507334
23andMers397507334
23andMe allrs397507334
SNP Nexus

SNPshotrs397507334
SNPdbers397507334
MSV3drs397507334
GWAS Ctlgrs397507334
Max Magnitude6
ClinVar
Risk rs397507334(A;A)
Alt rs397507334(A;A)
Reference Rs397507334(-;-)
Significance Pathogenic
Disease Breast-ovarian cancer not provided
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 not provided
Reversed 0
HGVS NC_000013.10:g.32912962dupA
CLNSRC ClinVar
CLNACC RCV000031486.4, RCV000485961.1,