Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1060502716

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060502716(A;A)
Make rs1060502716(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome22
Position28695874
GeneCHEK2
is asnp
is mentioned by
dbSNPrs1060502716
dbSNP (old)rs1060502716
ClinGenrs1060502716
ebirs1060502716
HLIrs1060502716
Exacrs1060502716
Gnomadrs1060502716
Varsomers1060502716
Maprs1060502716
PheGenIrs1060502716
Biobankrs1060502716
1000 genomesrs1060502716
hgdprs1060502716
ensemblrs1060502716
gopubmedrs1060502716
geneviewrs1060502716
scholarrs1060502716
googlers1060502716
pharmgkbrs1060502716
gwascentralrs1060502716
openSNPrs1060502716
23andMers1060502716
23andMe allrs1060502716
SNPshotrs1060502716
SNPdbers1060502716
MSV3drs1060502716
GWAS Ctlgrs1060502716
Max Magnitude0
ClinVar
Risk rs1060502716(A;A)
Alt rs1060502716(A;A)
Reference Rs1060502716(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.29091862C>T
CLNSRC
CLNACC RCV000464247.1,