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rs397507811

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397507811(-;-)
Make rs397507811(-;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340253
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507811
ebirs397507811
HLIrs397507811
Exacrs397507811
Varsomers397507811
Maprs397507811
PheGenIrs397507811
hapmaprs397507811
1000 genomesrs397507811
hgdprs397507811
ensemblrs397507811
gopubmedrs397507811
geneviewrs397507811
scholarrs397507811
googlers397507811
pharmgkbrs397507811
gwascentralrs397507811
openSNPrs397507811
23andMers397507811
23andMe allrs397507811
SNP Nexus

SNPshotrs397507811
SNPdbers397507811
MSV3drs397507811
GWAS Ctlgrs397507811
Max Magnitude0
ClinVar
Risk rs397507811(;)
Alt rs397507811(;)
Reference rs397507811(T;T)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32914390delT
CLNSRC ClinVar
CLNACC RCV000044789.2,