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rs397507375

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;GA) 6 BRCA2 variant considered pathogenic for breast cancer
(AG;AG) 0 common in clinvar
(GA;GA) 0 common in clinvar


Make rs397507375(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32341079
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507375
dbSNP (old)rs397507375
ClinGenrs397507375
ebirs397507375
HLIrs397507375
Exacrs397507375
Gnomadrs397507375
Varsomers397507375
Maprs397507375
PheGenIrs397507375
Biobankrs397507375
1000 genomesrs397507375
hgdprs397507375
ensemblrs397507375
gopubmedrs397507375
geneviewrs397507375
scholarrs397507375
googlers397507375
pharmgkbrs397507375
gwascentralrs397507375
openSNPrs397507375
23andMers397507375
23andMe allrs397507375
SNP Nexus

SNPshotrs397507375
SNPdbers397507375
MSV3drs397507375
GWAS Ctlgrs397507375
Max Magnitude6
ClinVar
Risk rs397507375(-;-)
Alt rs397507375(-;-)
Reference Rs397507375(AG;AG)
Significance Pathogenic
Disease Breast-ovarian cancer Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32915216_32915217delGA
CLNSRC ClinVar
CLNACC RCV000031644.5, RCV000045032.2,