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

rs397507892

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397507892(-;-)
Make rs397507892(-;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position32330939
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507892
ebirs397507892
HLIrs397507892
Exacrs397507892
Varsomers397507892
Maprs397507892
PheGenIrs397507892
hapmaprs397507892
1000 genomesrs397507892
hgdprs397507892
ensemblrs397507892
gopubmedrs397507892
geneviewrs397507892
scholarrs397507892
googlers397507892
pharmgkbrs397507892
gwascentralrs397507892
openSNPrs397507892
23andMers397507892
23andMe allrs397507892
SNP Nexus

SNPshotrs397507892
SNPdbers397507892
MSV3drs397507892
GWAS Ctlgrs397507892
Max Magnitude0
ClinVar
Risk rs397507892(;)
Alt rs397507892(;)
Reference rs397507892(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.32905076delC
CLNSRC ClinVar
CLNACC RCV000045124.2,