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

rs397507755

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507755(-;-)
Make rs397507755(-;T)
Make rs397507755(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339369
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507755
ebirs397507755
HLIrs397507755
Exacrs397507755
Varsomers397507755
Maprs397507755
PheGenIrs397507755
hapmaprs397507755
1000 genomesrs397507755
hgdprs397507755
ensemblrs397507755
gopubmedrs397507755
geneviewrs397507755
scholarrs397507755
googlers397507755
pharmgkbrs397507755
gwascentralrs397507755
openSNPrs397507755
23andMers397507755
23andMe allrs397507755
SNP Nexus

SNPshotrs397507755
SNPdbers397507755
MSV3drs397507755
GWAS Ctlgrs397507755
Max Magnitude0
ClinVar
Risk rs397507755(T;T)
Alt rs397507755(T;T)
Reference rs397507755(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32913506dupT
CLNSRC ClinVar
CLNACC RCV000044538.2,