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rs397507699

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397507699(-;-)
Make rs397507699(-;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position32338284
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507699
ebirs397507699
HLIrs397507699
Exacrs397507699
Varsomers397507699
Maprs397507699
PheGenIrs397507699
hapmaprs397507699
1000 genomesrs397507699
hgdprs397507699
ensemblrs397507699
gopubmedrs397507699
geneviewrs397507699
scholarrs397507699
googlers397507699
pharmgkbrs397507699
gwascentralrs397507699
openSNPrs397507699
23andMers397507699
23andMe allrs397507699
SNP Nexus

SNPshotrs397507699
SNPdbers397507699
MSV3drs397507699
GWAS Ctlgrs397507699
Max Magnitude0
ClinVar
Risk rs397507699(;)
Alt rs397507699(;)
Reference rs397507699(C;C)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32912421delC
CLNSRC ClinVar
CLNACC RCV000044313.2,