Have questions? Visit https://www.reddit.com/r/SNPedia

rs397507853

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507853(-;-)
Make rs397507853(-;G)
Make rs397507853(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340777
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507853
ebirs397507853
HLIrs397507853
Exacrs397507853
Varsomers397507853
Maprs397507853
PheGenIrs397507853
hapmaprs397507853
1000 genomesrs397507853
hgdprs397507853
ensemblrs397507853
gopubmedrs397507853
geneviewrs397507853
scholarrs397507853
googlers397507853
pharmgkbrs397507853
gwascentralrs397507853
openSNPrs397507853
23andMers397507853
23andMe allrs397507853
SNP Nexus

SNPshotrs397507853
SNPdbers397507853
MSV3drs397507853
GWAS Ctlgrs397507853
Max Magnitude0
ClinVar
Risk rs397507853(G;G)
Alt rs397507853(G;G)
Reference rs397507853(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32914914dupG
CLNSRC ClinVar
CLNACC RCV000044942.2,