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rs397507959

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507959(-;-)
Make rs397507959(-;A)
Make rs397507959(A;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32363255
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507959
ebirs397507959
HLIrs397507959
Exacrs397507959
Varsomers397507959
Maprs397507959
PheGenIrs397507959
hapmaprs397507959
1000 genomesrs397507959
hgdprs397507959
ensemblrs397507959
gopubmedrs397507959
geneviewrs397507959
scholarrs397507959
googlers397507959
pharmgkbrs397507959
gwascentralrs397507959
openSNPrs397507959
23andMers397507959
23andMe allrs397507959
SNP Nexus

SNPshotrs397507959
SNPdbers397507959
MSV3drs397507959
GWAS Ctlgrs397507959
Max Magnitude0
ClinVar
Risk rs397507959(A;A)
Alt rs397507959(A;A)
Reference rs397507959(;)
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.32937392dupA
CLNSRC ClinVar
CLNACC RCV000045403.3,