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rs587781269

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587781269(C;T)
Make rs587781269(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome22
Position28734439
GeneCHEK2
is asnp
is mentioned by
dbSNPrs587781269
ebirs587781269
HLIrs587781269
Exacrs587781269
Varsomers587781269
Maprs587781269
PheGenIrs587781269
hapmaprs587781269
1000 genomesrs587781269
hgdprs587781269
ensemblrs587781269
gopubmedrs587781269
geneviewrs587781269
scholarrs587781269
googlers587781269
pharmgkbrs587781269
gwascentralrs587781269
openSNPrs587781269
23andMers587781269
23andMe allrs587781269
SNP Nexus

SNPshotrs587781269
SNPdbers587781269
MSV3drs587781269
GWAS Ctlgrs587781269
Max Magnitude0
ClinVar
Risk rs587781269(T;T)
Alt rs587781269(T;T)
Reference rs587781269(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided Familial cancer of breast
Variation info
Gene CHEK2
CLNDBN Hereditary cancer-predisposing syndrome not provided Familial cancer of breast
Reversed 1
HGVS NC_000022.10:g.29130427G>A
CLNSRC
CLNACC RCV000128901.2, RCV000215973.1, RCV000232015.1,