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rs397507850

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs397507850(-;-)
Make rs397507850(-;TT)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340761
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507850
ebirs397507850
HLIrs397507850
Exacrs397507850
Varsomers397507850
Maprs397507850
PheGenIrs397507850
hapmaprs397507850
1000 genomesrs397507850
hgdprs397507850
ensemblrs397507850
gopubmedrs397507850
geneviewrs397507850
scholarrs397507850
googlers397507850
pharmgkbrs397507850
gwascentralrs397507850
openSNPrs397507850
23andMers397507850
23andMe allrs397507850
SNP Nexus

SNPshotrs397507850
SNPdbers397507850
MSV3drs397507850
GWAS Ctlgrs397507850
Max Magnitude0
ClinVar
Risk rs397507850(;)
Alt rs397507850(;)
Reference rs397507850(TT;TT)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32914898_32914899delTT
CLNSRC ClinVar
CLNACC RCV000044935.2,