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rs397507650

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507650(-;-)
Make rs397507650(-;TT)
Make rs397507650(TT;TT)
ReferenceGRCh38 38.1/141
Chromosome13
Position32337370
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507650
ebirs397507650
HLIrs397507650
Exacrs397507650
Varsomers397507650
Maprs397507650
PheGenIrs397507650
hapmaprs397507650
1000 genomesrs397507650
hgdprs397507650
ensemblrs397507650
gopubmedrs397507650
geneviewrs397507650
scholarrs397507650
googlers397507650
pharmgkbrs397507650
gwascentralrs397507650
openSNPrs397507650
23andMers397507650
23andMe allrs397507650
SNP Nexus

SNPshotrs397507650
SNPdbers397507650
MSV3drs397507650
GWAS Ctlgrs397507650
Max Magnitude0
ClinVar
Risk rs397507650(TT;TT)
Alt rs397507650(TT;TT)
Reference rs397507650(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32911506_32911507dupTT
CLNSRC ClinVar
CLNACC RCV000044103.2,