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rs397507733

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507733(-;-)
Make rs397507733(-;T)
Make rs397507733(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32338993
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507733
ebirs397507733
HLIrs397507733
Exacrs397507733
Varsomers397507733
Maprs397507733
PheGenIrs397507733
hapmaprs397507733
1000 genomesrs397507733
hgdprs397507733
ensemblrs397507733
gopubmedrs397507733
geneviewrs397507733
scholarrs397507733
googlers397507733
pharmgkbrs397507733
gwascentralrs397507733
openSNPrs397507733
23andMers397507733
23andMe allrs397507733
SNP Nexus

SNPshotrs397507733
SNPdbers397507733
MSV3drs397507733
GWAS Ctlgrs397507733
Max Magnitude0
ClinVar
Risk rs397507733(T;T)
Alt rs397507733(T;T)
Reference Rs397507733(;)
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.32913130dupT
CLNSRC ClinVar
CLNACC RCV000044458.3,