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rs587780174

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587780174(-;-)
Make rs587780174(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome22
Position28695239
GeneCHEK2
is asnp
is mentioned by
dbSNPrs587780174
ebirs587780174
HLIrs587780174
Exacrs587780174
Varsomers587780174
Maprs587780174
PheGenIrs587780174
hapmaprs587780174
1000 genomesrs587780174
hgdprs587780174
ensemblrs587780174
gopubmedrs587780174
geneviewrs587780174
scholarrs587780174
googlers587780174
pharmgkbrs587780174
gwascentralrs587780174
openSNPrs587780174
23andMers587780174
23andMe allrs587780174
SNP Nexus

SNPshotrs587780174
SNPdbers587780174
MSV3drs587780174
GWAS Ctlgrs587780174
Max Magnitude0
ClinVar
Risk rs587780174(;)
Alt rs587780174(;)
Reference rs587780174(T;T)
Significance 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.29091227delA
CLNSRC
CLNACC RCV000115992.5, RCV000198820.2, RCV000212457.1,