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

rs397507928

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507928(-;-)
Make rs397507928(-;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32357795
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507928
ebirs397507928
HLIrs397507928
Exacrs397507928
Varsomers397507928
Maprs397507928
PheGenIrs397507928
hapmaprs397507928
1000 genomesrs397507928
hgdprs397507928
ensemblrs397507928
gopubmedrs397507928
geneviewrs397507928
scholarrs397507928
googlers397507928
pharmgkbrs397507928
gwascentralrs397507928
openSNPrs397507928
23andMers397507928
23andMe allrs397507928
SNP Nexus

SNPshotrs397507928
SNPdbers397507928
MSV3drs397507928
GWAS Ctlgrs397507928
Max Magnitude0
ClinVar
Risk rs397507928(;)
Alt rs397507928(;)
Reference rs397507928(A;A)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32931932delA
CLNSRC ClinVar
CLNACC RCV000045278.2,