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rs397507894

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs397507894(-;-)
Make rs397507894(-;TT)
ReferenceGRCh38 38.1/141
Chromosome13
Position32354920
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507894
ebirs397507894
HLIrs397507894
Exacrs397507894
Varsomers397507894
Maprs397507894
PheGenIrs397507894
hapmaprs397507894
1000 genomesrs397507894
hgdprs397507894
ensemblrs397507894
gopubmedrs397507894
geneviewrs397507894
scholarrs397507894
googlers397507894
pharmgkbrs397507894
gwascentralrs397507894
openSNPrs397507894
23andMers397507894
23andMe allrs397507894
SNP Nexus

SNPshotrs397507894
SNPdbers397507894
MSV3drs397507894
GWAS Ctlgrs397507894
Max Magnitude0
ClinVar
Risk rs397507894(;)
Alt rs397507894(;)
Reference rs397507894(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.32929057_32929058delTT
CLNSRC ClinVar
CLNACC RCV000045135.2,