Have questions? Visit https://www.reddit.com/r/SNPedia

rs397507265

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397507265(-;-)
Make rs397507265(-;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32332683
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507265
ebirs397507265
HLIrs397507265
Exacrs397507265
Varsomers397507265
Maprs397507265
PheGenIrs397507265
hapmaprs397507265
1000 genomesrs397507265
hgdprs397507265
ensemblrs397507265
gopubmedrs397507265
geneviewrs397507265
scholarrs397507265
googlers397507265
pharmgkbrs397507265
gwascentralrs397507265
openSNPrs397507265
23andMers397507265
23andMe allrs397507265
SNP Nexus

SNPshotrs397507265
SNPdbers397507265
MSV3drs397507265
GWAS Ctlgrs397507265
Max Magnitude0
ClinVar
Risk rs397507265(;)
Alt rs397507265(;)
Reference rs397507265(G;G)
Significance Pathogenic
Disease Breast-ovarian cancer Hereditary cancer-predisposing syndrome not provided
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000013.10:g.32906820delG
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000031311.3, RCV000129350.2, RCV000160276.2,