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rs753159426

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs753159426(-;-)
Make rs753159426(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position28695781
GeneCHEK2
is asnp
is mentioned by
dbSNPrs753159426
ebirs753159426
HLIrs753159426
Exacrs753159426
Varsomers753159426
Maprs753159426
PheGenIrs753159426
hapmaprs753159426
1000 genomesrs753159426
hgdprs753159426
ensemblrs753159426
gopubmedrs753159426
geneviewrs753159426
scholarrs753159426
googlers753159426
pharmgkbrs753159426
gwascentralrs753159426
openSNPrs753159426
23andMers753159426
23andMe allrs753159426
SNP Nexus

SNPshotrs753159426
SNPdbers753159426
MSV3drs753159426
GWAS Ctlgrs753159426
Max Magnitude0
ClinVar
Risk rs753159426(;)
Alt rs753159426(;)
Reference rs753159426(A;A)
Significance Pathogenic
Disease Familial cancer of breast
Variation info
Gene CHEK2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000022.10:g.29091769delA
CLNSRC
CLNACC RCV000234460.1,