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

rs1057517596

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517596(-;-)
Make rs1057517596(-;G)
ReferenceGRCh38.p7 38.3/150
Chromosome22
Position28699937
GeneCHEK2
is asnp
is mentioned by
dbSNPrs1057517596
dbSNP (old)rs1057517596
ClinGenrs1057517596
ebirs1057517596
HLIrs1057517596
Exacrs1057517596
Gnomadrs1057517596
Varsomers1057517596
Maprs1057517596
PheGenIrs1057517596
Biobankrs1057517596
1000 genomesrs1057517596
hgdprs1057517596
ensemblrs1057517596
gopubmedrs1057517596
geneviewrs1057517596
scholarrs1057517596
googlers1057517596
pharmgkbrs1057517596
gwascentralrs1057517596
openSNPrs1057517596
23andMers1057517596
23andMe allrs1057517596
SNPshotrs1057517596
SNPdbers1057517596
MSV3drs1057517596
GWAS Ctlgrs1057517596
Max Magnitude0
ClinVar
Risk rs1057517596(-;-)
Alt rs1057517596(-;-)
Reference Rs1057517596(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.29095925delC
CLNSRC
CLNACC RCV000409709.1,