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rs397507848

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507848(-;-)
Make rs397507848(-;T)
Make rs397507848(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340745
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507848
ebirs397507848
HLIrs397507848
Exacrs397507848
Varsomers397507848
Maprs397507848
PheGenIrs397507848
hapmaprs397507848
1000 genomesrs397507848
hgdprs397507848
ensemblrs397507848
gopubmedrs397507848
geneviewrs397507848
scholarrs397507848
googlers397507848
pharmgkbrs397507848
gwascentralrs397507848
openSNPrs397507848
23andMers397507848
23andMe allrs397507848
SNP Nexus

SNPshotrs397507848
SNPdbers397507848
MSV3drs397507848
GWAS Ctlgrs397507848
Max Magnitude0
ClinVar
Risk rs397507848(T;T)
Alt rs397507848(T;T)
Reference rs397507848(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32914882dupT
CLNSRC ClinVar
CLNACC RCV000044929.2,