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rs397507644

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397507644(-;-)
Make rs397507644(-;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32337200
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507644
ebirs397507644
HLIrs397507644
Exacrs397507644
Varsomers397507644
Maprs397507644
PheGenIrs397507644
hapmaprs397507644
1000 genomesrs397507644
hgdprs397507644
ensemblrs397507644
gopubmedrs397507644
geneviewrs397507644
scholarrs397507644
googlers397507644
pharmgkbrs397507644
gwascentralrs397507644
openSNPrs397507644
23andMers397507644
23andMe allrs397507644
SNP Nexus

SNPshotrs397507644
SNPdbers397507644
MSV3drs397507644
GWAS Ctlgrs397507644
Max Magnitude0
ClinVar
Risk rs397507644(;)
Alt rs397507644(;)
Reference rs397507644(T;T)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32911337delT
CLNSRC ClinVar
CLNACC RCV000044074.2,