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rs786203458

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786203458(-;-)
Make rs786203458(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome22
Position28734445
GeneCHEK2
is asnp
is mentioned by
dbSNPrs786203458
ebirs786203458
HLIrs786203458
Exacrs786203458
Varsomers786203458
Maprs786203458
PheGenIrs786203458
hapmaprs786203458
1000 genomesrs786203458
hgdprs786203458
ensemblrs786203458
gopubmedrs786203458
geneviewrs786203458
scholarrs786203458
googlers786203458
pharmgkbrs786203458
gwascentralrs786203458
openSNPrs786203458
23andMers786203458
23andMe allrs786203458
SNP Nexus

SNPshotrs786203458
SNPdbers786203458
MSV3drs786203458
GWAS Ctlgrs786203458
Max Magnitude0
ClinVar
Risk rs786203458(;)
Alt rs786203458(;)
Reference rs786203458(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Familial cancer of breast not provided
Variation info
Gene CHEK2
CLNDBN Hereditary cancer-predisposing syndrome Familial cancer of breast not provided
Reversed 1
HGVS NC_000022.10:g.29130433delA
CLNSRC
CLNACC RCV000166773.1, RCV000197766.3, RCV000223102.1,