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rs397507669

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507669(-;-)
Make rs397507669(-;T)
Make rs397507669(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32337807
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507669
ebirs397507669
HLIrs397507669
Exacrs397507669
Varsomers397507669
Maprs397507669
PheGenIrs397507669
hapmaprs397507669
1000 genomesrs397507669
hgdprs397507669
ensemblrs397507669
gopubmedrs397507669
geneviewrs397507669
scholarrs397507669
googlers397507669
pharmgkbrs397507669
gwascentralrs397507669
openSNPrs397507669
23andMers397507669
23andMe allrs397507669
SNP Nexus

SNPshotrs397507669
SNPdbers397507669
MSV3drs397507669
GWAS Ctlgrs397507669
Max Magnitude0
ClinVar
Risk rs397507669(T;T)
Alt rs397507669(T;T)
Reference rs397507669(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32911944dupT
CLNSRC ClinVar
CLNACC RCV000044198.2,