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rs397507573

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397507573(-;-)
Make rs397507573(-;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32319124
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507573
ClinGenrs397507573
ebirs397507573
HLIrs397507573
Exacrs397507573
Varsomers397507573
Maprs397507573
PheGenIrs397507573
hapmaprs397507573
1000 genomesrs397507573
hgdprs397507573
ensemblrs397507573
gopubmedrs397507573
geneviewrs397507573
scholarrs397507573
googlers397507573
pharmgkbrs397507573
gwascentralrs397507573
openSNPrs397507573
23andMers397507573
23andMe allrs397507573
SNP Nexus

SNPshotrs397507573
SNPdbers397507573
MSV3drs397507573
GWAS Ctlgrs397507573
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs397507573(G;G)
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.32893261delG
CLNSRC ClinVar
CLNACC RCV000043749.2, RCV000241066.2,