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rs397507962

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507962(-;-)
Make rs397507962(-;TT)
Make rs397507962(TT;TT)
ReferenceGRCh38 38.1/141
Chromosome13
Position32363273
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507962
ebirs397507962
HLIrs397507962
Exacrs397507962
Varsomers397507962
Maprs397507962
PheGenIrs397507962
hapmaprs397507962
1000 genomesrs397507962
hgdprs397507962
ensemblrs397507962
gopubmedrs397507962
geneviewrs397507962
scholarrs397507962
googlers397507962
pharmgkbrs397507962
gwascentralrs397507962
openSNPrs397507962
23andMers397507962
23andMe allrs397507962
SNP Nexus

SNPshotrs397507962
SNPdbers397507962
MSV3drs397507962
GWAS Ctlgrs397507962
Max Magnitude0
ClinVar
Risk rs397507962(TT;TT)
Alt rs397507962(TT;TT)
Reference rs397507962(;)
Significance Pathogenic
Disease Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000013.10:g.32937409_32937410dupTT
CLNSRC ClinVar
CLNACC RCV000045413.3,