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rs397508039

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508039(-;-)
Make rs397508039(-;T)
Make rs397508039(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32332396
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508039
ebirs397508039
HLIrs397508039
Exacrs397508039
Varsomers397508039
Maprs397508039
PheGenIrs397508039
hapmaprs397508039
1000 genomesrs397508039
hgdprs397508039
ensemblrs397508039
gopubmedrs397508039
geneviewrs397508039
scholarrs397508039
googlers397508039
pharmgkbrs397508039
gwascentralrs397508039
openSNPrs397508039
23andMers397508039
23andMe allrs397508039
SNP Nexus

SNPshotrs397508039
SNPdbers397508039
MSV3drs397508039
GWAS Ctlgrs397508039
Max Magnitude0
ClinVar
Risk rs397508039(T;T)
Alt rs397508039(T;T)
Reference rs397508039(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32906533dupT
CLNSRC ClinVar
CLNACC RCV000045741.2,