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rs786203889

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786203889(A;A)
Make rs786203889(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome22
Position28734444
GeneCHEK2
is asnp
is mentioned by
dbSNPrs786203889
ebirs786203889
HLIrs786203889
Exacrs786203889
Varsomers786203889
Maprs786203889
PheGenIrs786203889
hapmaprs786203889
1000 genomesrs786203889
hgdprs786203889
ensemblrs786203889
gopubmedrs786203889
geneviewrs786203889
scholarrs786203889
googlers786203889
pharmgkbrs786203889
gwascentralrs786203889
openSNPrs786203889
23andMers786203889
23andMe allrs786203889
SNP Nexus

SNPshotrs786203889
SNPdbers786203889
MSV3drs786203889
GWAS Ctlgrs786203889
Max Magnitude0
ClinVar
Risk rs786203889(A;A)
Alt rs786203889(A;A)
Reference rs786203889(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene CHEK2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000022.10:g.29130432C>T
CLNSRC
CLNACC RCV000167390.1,