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rs786203650

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786203650(G;T)
Make rs786203650(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome22
Position28719394
GeneCHEK2
is asnp
is mentioned by
dbSNPrs786203650
ebirs786203650
HLIrs786203650
Exacrs786203650
Varsomers786203650
Maprs786203650
PheGenIrs786203650
hapmaprs786203650
1000 genomesrs786203650
hgdprs786203650
ensemblrs786203650
gopubmedrs786203650
geneviewrs786203650
scholarrs786203650
googlers786203650
pharmgkbrs786203650
gwascentralrs786203650
openSNPrs786203650
23andMers786203650
23andMe allrs786203650
SNP Nexus

SNPshotrs786203650
SNPdbers786203650
MSV3drs786203650
GWAS Ctlgrs786203650
Max Magnitude0
ClinVar
Risk rs786203650(T;T)
Alt rs786203650(T;T)
Reference rs786203650(G;G)
Significance Probable-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.29115382C>A; NC_000022.10:g.29115382C>T
CLNSRC
CLNACC RCV000167053.1, RCV000204794.1, RCV000216702.1, RCV000229878.1,