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rs397507653

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507653(-;-)
Make rs397507653(-;A)
Make rs397507653(A;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32337423
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507653
ebirs397507653
HLIrs397507653
Exacrs397507653
Varsomers397507653
Maprs397507653
PheGenIrs397507653
hapmaprs397507653
1000 genomesrs397507653
hgdprs397507653
ensemblrs397507653
gopubmedrs397507653
geneviewrs397507653
scholarrs397507653
googlers397507653
pharmgkbrs397507653
gwascentralrs397507653
openSNPrs397507653
23andMers397507653
23andMe allrs397507653
SNP Nexus

SNPshotrs397507653
SNPdbers397507653
MSV3drs397507653
GWAS Ctlgrs397507653
Max Magnitude0
ClinVar
Risk rs397507653(A;A)
Alt rs397507653(A;A)
Reference rs397507653(;)
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.32911560dupA
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000044110.2, RCV000113129.1,