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rs397507898

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397507898(-;-)
Make rs397507898(-;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32355019
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507898
ebirs397507898
HLIrs397507898
Exacrs397507898
Varsomers397507898
Maprs397507898
PheGenIrs397507898
hapmaprs397507898
1000 genomesrs397507898
hgdprs397507898
ensemblrs397507898
gopubmedrs397507898
geneviewrs397507898
scholarrs397507898
googlers397507898
pharmgkbrs397507898
gwascentralrs397507898
openSNPrs397507898
23andMers397507898
23andMe allrs397507898
SNP Nexus

SNPshotrs397507898
SNPdbers397507898
MSV3drs397507898
GWAS Ctlgrs397507898
Max Magnitude0
ClinVar
Risk rs397507898(;)
Alt rs397507898(;)
Reference rs397507898(G;G)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32929156delG
CLNSRC ClinVar
CLNACC RCV000045153.2,