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rs397508027

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(ATA;ATA) 0 common in clinvar
Make rs397508027(ATA;TT)
Make rs397508027(TT;TT)
ReferenceGRCh38 38.1/141
Chromosome13
Position32379784
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508027
ebirs397508027
HLIrs397508027
Exacrs397508027
Varsomers397508027
Maprs397508027
PheGenIrs397508027
hapmaprs397508027
1000 genomesrs397508027
hgdprs397508027
ensemblrs397508027
gopubmedrs397508027
geneviewrs397508027
scholarrs397508027
googlers397508027
pharmgkbrs397508027
gwascentralrs397508027
openSNPrs397508027
23andMers397508027
23andMe allrs397508027
SNP Nexus

SNPshotrs397508027
SNPdbers397508027
MSV3drs397508027
GWAS Ctlgrs397508027
Max Magnitude0
ClinVar
Risk rs397508027(TT;TT)
Alt rs397508027(TT;TT)
Reference rs397508027(ATA;ATA)
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.32953921_32953923delATAinsTT
CLNSRC ClinVar
CLNACC RCV000045681.2,