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rs397507701

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
(-;A) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs397507701(A;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32338360
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507701
dbSNP (old)rs397507701
ClinGenrs397507701
ebirs397507701
HLIrs397507701
Exacrs397507701
Varsomers397507701
Maprs397507701
PheGenIrs397507701
Biobankrs397507701
1000 genomesrs397507701
hgdprs397507701
ensemblrs397507701
gopubmedrs397507701
geneviewrs397507701
scholarrs397507701
googlers397507701
pharmgkbrs397507701
gwascentralrs397507701
openSNPrs397507701
23andMers397507701
23andMe allrs397507701
SNP Nexus

SNPshotrs397507701
SNPdbers397507701
MSV3drs397507701
GWAS Ctlgrs397507701
Max Magnitude6
ClinVar
Risk rs397507701(A;A)
Alt rs397507701(A;A)
Reference Rs397507701(-;-)
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.32912497dupA
CLNSRC ClinVar
CLNACC RCV000044331.2, RCV000256647.2,