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

rs397507980

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507980(-;-)
Make rs397507980(-;C)
Make rs397507980(C;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position32370418
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507980
ebirs397507980
HLIrs397507980
Exacrs397507980
Varsomers397507980
Maprs397507980
PheGenIrs397507980
hapmaprs397507980
1000 genomesrs397507980
hgdprs397507980
ensemblrs397507980
gopubmedrs397507980
geneviewrs397507980
scholarrs397507980
googlers397507980
pharmgkbrs397507980
gwascentralrs397507980
openSNPrs397507980
23andMers397507980
23andMe allrs397507980
SNP Nexus

SNPshotrs397507980
SNPdbers397507980
MSV3drs397507980
GWAS Ctlgrs397507980
Max Magnitude0
ClinVar
Risk rs397507980(C;C)
Alt rs397507980(C;C)
Reference rs397507980(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32944555dupC
CLNSRC ClinVar
CLNACC RCV000045486.2,