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rs786203229

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786203229(A;A)
Make rs786203229(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome22
Position28719486
GeneCHEK2
is asnp
is mentioned by
dbSNPrs786203229
ebirs786203229
HLIrs786203229
Exacrs786203229
Varsomers786203229
Maprs786203229
PheGenIrs786203229
hapmaprs786203229
1000 genomesrs786203229
hgdprs786203229
ensemblrs786203229
gopubmedrs786203229
geneviewrs786203229
scholarrs786203229
googlers786203229
pharmgkbrs786203229
gwascentralrs786203229
openSNPrs786203229
23andMers786203229
23andMe allrs786203229
SNP Nexus

SNPshotrs786203229
SNPdbers786203229
MSV3drs786203229
GWAS Ctlgrs786203229
Max Magnitude0
ClinVar
Risk rs786203229(A;A)
Alt rs786203229(A;A)
Reference rs786203229(G;G)
Significance Probable-Pathogenic
Disease Familial cancer of breast Hereditary cancer-predisposing syndrome
Variation info
Gene CHEK2
CLNDBN Familial cancer of breast Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000022.10:g.29115474C>A; NC_000022.10:g.29115474C>T
CLNSRC
CLNACC RCV000195929.1, RCV000166451.1,