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rs1060502710

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060502710(A;A)
Make rs1060502710(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome22
Position28711922
GeneCHEK2
is asnp
is mentioned by
dbSNPrs1060502710
dbSNP (old)rs1060502710
ClinGenrs1060502710
ebirs1060502710
HLIrs1060502710
Exacrs1060502710
Gnomadrs1060502710
Varsomers1060502710
LitVarrs1060502710
Maprs1060502710
PheGenIrs1060502710
Biobankrs1060502710
1000 genomesrs1060502710
hgdprs1060502710
ensemblrs1060502710
gopubmedrs1060502710
geneviewrs1060502710
scholarrs1060502710
googlers1060502710
pharmgkbrs1060502710
gwascentralrs1060502710
openSNPrs1060502710
23andMers1060502710
23andMe allrs1060502710
SNPshotrs1060502710
SNPdbers1060502710
MSV3drs1060502710
GWAS Ctlgrs1060502710
Max Magnitude0
ClinVar
Risk rs1060502710(A;A)
Alt rs1060502710(A;A)
Reference Rs1060502710(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.29107910G>T
CLNSRC
CLNACC RCV000460369.1,