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rs786202601

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786202601(-;-)
Make rs786202601(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome22
Position28694059
GeneCHEK2
is asnp
is mentioned by
dbSNPrs786202601
ebirs786202601
HLIrs786202601
Exacrs786202601
Varsomers786202601
Maprs786202601
PheGenIrs786202601
hapmaprs786202601
1000 genomesrs786202601
hgdprs786202601
ensemblrs786202601
gopubmedrs786202601
geneviewrs786202601
scholarrs786202601
googlers786202601
pharmgkbrs786202601
gwascentralrs786202601
openSNPrs786202601
23andMers786202601
23andMe allrs786202601
SNP Nexus

SNPshotrs786202601
SNPdbers786202601
MSV3drs786202601
GWAS Ctlgrs786202601
Max Magnitude0
ClinVar
Risk rs786202601(;)
Alt rs786202601(;)
Reference rs786202601(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene CHEK2
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 1
HGVS NC_000022.10:g.29090047delT
CLNSRC
CLNACC RCV000165489.1, RCV000222773.1,