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rs1060502711

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060502711(-;-)
Make rs1060502711(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome22
Position28734446
GeneCHEK2
is asnp
is mentioned by
dbSNPrs1060502711
dbSNP (old)rs1060502711
ClinGenrs1060502711
ebirs1060502711
HLIrs1060502711
Exacrs1060502711
Gnomadrs1060502711
Varsomers1060502711
Maprs1060502711
PheGenIrs1060502711
Biobankrs1060502711
1000 genomesrs1060502711
hgdprs1060502711
ensemblrs1060502711
gopubmedrs1060502711
geneviewrs1060502711
scholarrs1060502711
googlers1060502711
pharmgkbrs1060502711
gwascentralrs1060502711
openSNPrs1060502711
23andMers1060502711
23andMe allrs1060502711
SNPshotrs1060502711
SNPdbers1060502711
MSV3drs1060502711
GWAS Ctlgrs1060502711
Max Magnitude0
ClinVar
Risk rs1060502711(-;-)
Alt rs1060502711(-;-)
Reference Rs1060502711(C;C)
Significance Pathogenic
Disease Familial cancer of breast
Variation info
Gene CHEK2
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000022.10:g.29130434delG
CLNSRC
CLNACC RCV000467195.1,