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rs397508018

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508018(-;-)
Make rs397508018(-;A)
Make rs397508018(A;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32379474
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508018
ebirs397508018
HLIrs397508018
Exacrs397508018
Varsomers397508018
Maprs397508018
PheGenIrs397508018
hapmaprs397508018
1000 genomesrs397508018
hgdprs397508018
ensemblrs397508018
gopubmedrs397508018
geneviewrs397508018
scholarrs397508018
googlers397508018
pharmgkbrs397508018
gwascentralrs397508018
openSNPrs397508018
23andMers397508018
23andMe allrs397508018
SNP Nexus

SNPshotrs397508018
SNPdbers397508018
MSV3drs397508018
GWAS Ctlgrs397508018
Max Magnitude0
ClinVar
Risk rs397508018(A;A)
Alt rs397508018(A;A)
Reference rs397508018(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32953611dupA
CLNSRC ClinVar
CLNACC RCV000045653.2,