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rs1064795959

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome22
Position28734440
GeneCHEK2
is asnp
is mentioned by
dbSNPrs1064795959
dbSNP (old)rs1064795959
ClinGenrs1064795959
ebirs1064795959
HLIrs1064795959
Exacrs1064795959
Gnomadrs1064795959
Varsomers1064795959
Maprs1064795959
PheGenIrs1064795959
Biobankrs1064795959
1000 genomesrs1064795959
hgdprs1064795959
ensemblrs1064795959
gopubmedrs1064795959
geneviewrs1064795959
scholarrs1064795959
googlers1064795959
pharmgkbrs1064795959
gwascentralrs1064795959
openSNPrs1064795959
23andMers1064795959
23andMe allrs1064795959
SNPshotrs1064795959
SNPdbers1064795959
MSV3drs1064795959
GWAS Ctlgrs1064795959
Max Magnitude0
ClinVar
Risk rs1064795959(-;-)
Alt rs1064795959(-;-)
Reference Rs1064795959(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CHEK2
CLNDBN not provided
Reversed 1
HGVS NC_000022.10:g.29130428delA
CLNSRC
CLNACC RCV000486640.1,