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rs587780186

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587780186(-;-)
Make rs587780186(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome22
Position28724988
GeneCHEK2
is asnp
is mentioned by
dbSNPrs587780186
ebirs587780186
HLIrs587780186
Exacrs587780186
Varsomers587780186
Maprs587780186
PheGenIrs587780186
hapmaprs587780186
1000 genomesrs587780186
hgdprs587780186
ensemblrs587780186
gopubmedrs587780186
geneviewrs587780186
scholarrs587780186
googlers587780186
pharmgkbrs587780186
gwascentralrs587780186
openSNPrs587780186
23andMers587780186
23andMe allrs587780186
SNP Nexus

SNPshotrs587780186
SNPdbers587780186
MSV3drs587780186
GWAS Ctlgrs587780186
Max Magnitude0
ClinVar
Risk rs587780186(;)
Alt rs587780186(;)
Reference rs587780186(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.29120976delC
CLNSRC
CLNACC RCV000116027.2,