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rs786201906

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786201906(A;A)
Make rs786201906(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome22
Position28695243
GeneCHEK2
is asnp
is mentioned by
dbSNPrs786201906
ebirs786201906
HLIrs786201906
Exacrs786201906
Varsomers786201906
Maprs786201906
PheGenIrs786201906
hapmaprs786201906
1000 genomesrs786201906
hgdprs786201906
ensemblrs786201906
gopubmedrs786201906
geneviewrs786201906
scholarrs786201906
googlers786201906
pharmgkbrs786201906
gwascentralrs786201906
openSNPrs786201906
23andMers786201906
23andMe allrs786201906
SNP Nexus

SNPshotrs786201906
SNPdbers786201906
MSV3drs786201906
GWAS Ctlgrs786201906
Max Magnitude0
ClinVar
Risk rs786201906(A;A)
Alt rs786201906(A;A)
Reference rs786201906(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene CHEK2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000022.10:g.29091231C>T
CLNSRC
CLNACC RCV000164426.1,