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

rs397507806

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397507806(-;-)
Make rs397507806(-;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340144
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507806
ebirs397507806
HLIrs397507806
Exacrs397507806
Varsomers397507806
Maprs397507806
PheGenIrs397507806
hapmaprs397507806
1000 genomesrs397507806
hgdprs397507806
ensemblrs397507806
gopubmedrs397507806
geneviewrs397507806
scholarrs397507806
googlers397507806
pharmgkbrs397507806
gwascentralrs397507806
openSNPrs397507806
23andMers397507806
23andMe allrs397507806
SNP Nexus

SNPshotrs397507806
SNPdbers397507806
MSV3drs397507806
GWAS Ctlgrs397507806
Max Magnitude0
ClinVar
Risk rs397507806(;)
Alt rs397507806(;)
Reference rs397507806(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.32914281delT
CLNSRC ClinVar
CLNACC RCV000044757.2,