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rs397507999

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507999(-;-)
Make rs397507999(-;TT)
Make rs397507999(TT;TT)
ReferenceGRCh38 38.1/141
Chromosome13
Position32376679
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507999
ebirs397507999
HLIrs397507999
Exacrs397507999
Varsomers397507999
Maprs397507999
PheGenIrs397507999
hapmaprs397507999
1000 genomesrs397507999
hgdprs397507999
ensemblrs397507999
gopubmedrs397507999
geneviewrs397507999
scholarrs397507999
googlers397507999
pharmgkbrs397507999
gwascentralrs397507999
openSNPrs397507999
23andMers397507999
23andMe allrs397507999
SNP Nexus

SNPshotrs397507999
SNPdbers397507999
MSV3drs397507999
GWAS Ctlgrs397507999
Max Magnitude0
ClinVar
Risk rs397507999(TT;TT)
Alt rs397507999(TT;TT)
Reference rs397507999(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32950816_32950817insTT
CLNSRC ClinVar
CLNACC RCV000045587.2,