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rs397507640

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507640(-;-)
Make rs397507640(-;T)
Make rs397507640(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32337128
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507640
ebirs397507640
HLIrs397507640
Exacrs397507640
Varsomers397507640
Maprs397507640
PheGenIrs397507640
hapmaprs397507640
1000 genomesrs397507640
hgdprs397507640
ensemblrs397507640
gopubmedrs397507640
geneviewrs397507640
scholarrs397507640
googlers397507640
pharmgkbrs397507640
gwascentralrs397507640
openSNPrs397507640
23andMers397507640
23andMe allrs397507640
SNP Nexus

SNPshotrs397507640
SNPdbers397507640
MSV3drs397507640
GWAS Ctlgrs397507640
Max Magnitude0
ClinVar
Risk rs397507640(T;T)
Alt rs397507640(T;T)
Reference rs397507640(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32911265dupT
CLNSRC ClinVar
CLNACC RCV000044053.2,