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rs397507715

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs397507715(-;-)
Make rs397507715(-;TT)
ReferenceGRCh38 38.1/141
Chromosome13
Position32338735
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507715
ebirs397507715
HLIrs397507715
Exacrs397507715
Varsomers397507715
Maprs397507715
PheGenIrs397507715
hapmaprs397507715
1000 genomesrs397507715
hgdprs397507715
ensemblrs397507715
gopubmedrs397507715
geneviewrs397507715
scholarrs397507715
googlers397507715
pharmgkbrs397507715
gwascentralrs397507715
openSNPrs397507715
23andMers397507715
23andMe allrs397507715
SNP Nexus

SNPshotrs397507715
SNPdbers397507715
MSV3drs397507715
GWAS Ctlgrs397507715
Max Magnitude0
ClinVar
Risk rs397507715(;)
Alt rs397507715(;)
Reference rs397507715(TT;TT)
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.32912872_32912873delTT
CLNSRC ClinVar
CLNACC RCV000044402.2, RCV000239281.1,