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rs397507787

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GT;GT) 0 common in clinvar
(TG;TG) 0 common in clinvar
Make rs397507787(-;-)
Make rs397507787(-;GT)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339915
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507787
ebirs397507787
HLIrs397507787
Exacrs397507787
Varsomers397507787
Maprs397507787
PheGenIrs397507787
hapmaprs397507787
1000 genomesrs397507787
hgdprs397507787
ensemblrs397507787
gopubmedrs397507787
geneviewrs397507787
scholarrs397507787
googlers397507787
pharmgkbrs397507787
gwascentralrs397507787
openSNPrs397507787
23andMers397507787
23andMe allrs397507787
SNP Nexus

SNPshotrs397507787
SNPdbers397507787
MSV3drs397507787
GWAS Ctlgrs397507787
Max Magnitude0
ClinVar
Risk rs397507787(;)
Alt rs397507787(;)
Reference rs397507787(TG;TG)
Significance Pathogenic
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32914052_32914053delGT
CLNSRC ClinVar
CLNACC RCV000044681.3,