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rs397507771

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507771(-;-)
Make rs397507771(-;T)
Make rs397507771(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339552
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507771
ebirs397507771
HLIrs397507771
Exacrs397507771
Varsomers397507771
Maprs397507771
PheGenIrs397507771
hapmaprs397507771
1000 genomesrs397507771
hgdprs397507771
ensemblrs397507771
gopubmedrs397507771
geneviewrs397507771
scholarrs397507771
googlers397507771
pharmgkbrs397507771
gwascentralrs397507771
openSNPrs397507771
23andMers397507771
23andMe allrs397507771
SNP Nexus

SNPshotrs397507771
SNPdbers397507771
MSV3drs397507771
GWAS Ctlgrs397507771
Max Magnitude0
ClinVar
Risk rs397507771(T;T)
Alt rs397507771(T;T)
Reference rs397507771(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32913689dupT
CLNSRC ClinVar
CLNACC RCV000044601.2,