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rs1060502698

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060502698(A;A)
Make rs1060502698(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome22
Position28689216
GeneCHEK2
is asnp
is mentioned by
dbSNPrs1060502698
dbSNP (old)rs1060502698
ClinGenrs1060502698
ebirs1060502698
HLIrs1060502698
Exacrs1060502698
Gnomadrs1060502698
Varsomers1060502698
LitVarrs1060502698
Maprs1060502698
PheGenIrs1060502698
Biobankrs1060502698
1000 genomesrs1060502698
hgdprs1060502698
ensemblrs1060502698
gopubmedrs1060502698
geneviewrs1060502698
scholarrs1060502698
googlers1060502698
pharmgkbrs1060502698
gwascentralrs1060502698
openSNPrs1060502698
23andMers1060502698
23andMe allrs1060502698
SNPshotrs1060502698
SNPdbers1060502698
MSV3drs1060502698
GWAS Ctlgrs1060502698
Max Magnitude0
ClinVar
Risk rs1060502698(A;A)
Alt rs1060502698(A;A)
Reference Rs1060502698(G;G)
Significance Probable-Pathogenic
Disease Familial cancer of breast
Variation info
Gene CHEK2
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000022.10:g.29085204C>T
CLNSRC
CLNACC RCV000474737.1,