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

rs397507598

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397507598(-;-)
Make rs397507598(-;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32333114
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507598
ebirs397507598
HLIrs397507598
Exacrs397507598
Varsomers397507598
Maprs397507598
PheGenIrs397507598
hapmaprs397507598
1000 genomesrs397507598
hgdprs397507598
ensemblrs397507598
gopubmedrs397507598
geneviewrs397507598
scholarrs397507598
googlers397507598
pharmgkbrs397507598
gwascentralrs397507598
openSNPrs397507598
23andMers397507598
23andMe allrs397507598
SNP Nexus

SNPshotrs397507598
SNPdbers397507598
MSV3drs397507598
GWAS Ctlgrs397507598
Max Magnitude0
ClinVar
Risk rs397507598(;)
Alt rs397507598(;)
Reference rs397507598(T;T)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32907251delT
CLNSRC ClinVar
CLNACC RCV000043849.2,