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rs397507916

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507916(-;-)
Make rs397507916(-;T)
Make rs397507916(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32355262
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507916
ebirs397507916
HLIrs397507916
Exacrs397507916
Varsomers397507916
Maprs397507916
PheGenIrs397507916
hapmaprs397507916
1000 genomesrs397507916
hgdprs397507916
ensemblrs397507916
gopubmedrs397507916
geneviewrs397507916
scholarrs397507916
googlers397507916
pharmgkbrs397507916
gwascentralrs397507916
openSNPrs397507916
23andMers397507916
23andMe allrs397507916
SNP Nexus

SNPshotrs397507916
SNPdbers397507916
MSV3drs397507916
GWAS Ctlgrs397507916
Max Magnitude0
ClinVar
Risk rs397507916(T;T)
Alt rs397507916(T;T)
Reference rs397507916(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32929399dupT
CLNSRC ClinVar
CLNACC RCV000045200.2,