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rs397507823

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs397507823(-;-)
Make rs397507823(-;TT)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340388
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507823
ebirs397507823
HLIrs397507823
Exacrs397507823
Varsomers397507823
Maprs397507823
PheGenIrs397507823
hapmaprs397507823
1000 genomesrs397507823
hgdprs397507823
ensemblrs397507823
gopubmedrs397507823
geneviewrs397507823
scholarrs397507823
googlers397507823
pharmgkbrs397507823
gwascentralrs397507823
openSNPrs397507823
23andMers397507823
23andMe allrs397507823
SNP Nexus

SNPshotrs397507823
SNPdbers397507823
MSV3drs397507823
GWAS Ctlgrs397507823
Max Magnitude0
ClinVar
Risk rs397507823(;)
Alt rs397507823(;)
Reference rs397507823(TT;TT)
Significance Pathogenic
Disease Familial cancer of breast Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32914525_32914526delTT
CLNSRC ClinVar
CLNACC RCV000044824.2, RCV000165674.1,