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rs397508022

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508022(-;-)
Make rs397508022(-;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32379512
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508022
ebirs397508022
HLIrs397508022
Exacrs397508022
Varsomers397508022
Maprs397508022
PheGenIrs397508022
hapmaprs397508022
1000 genomesrs397508022
hgdprs397508022
ensemblrs397508022
gopubmedrs397508022
geneviewrs397508022
scholarrs397508022
googlers397508022
pharmgkbrs397508022
gwascentralrs397508022
openSNPrs397508022
23andMers397508022
23andMe allrs397508022
SNP Nexus

SNPshotrs397508022
SNPdbers397508022
MSV3drs397508022
GWAS Ctlgrs397508022
Max Magnitude0
ClinVar
Risk rs397508022(;)
Alt rs397508022(;)
Reference rs397508022(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.32953649delT
CLNSRC ClinVar
CLNACC RCV000045664.2,