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rs1064793817

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome22
Position28734694
GeneCHEK2
is asnp
is mentioned by
dbSNPrs1064793817
dbSNP (old)rs1064793817
ClinGenrs1064793817
ebirs1064793817
HLIrs1064793817
Exacrs1064793817
Gnomadrs1064793817
Varsomers1064793817
Maprs1064793817
PheGenIrs1064793817
Biobankrs1064793817
1000 genomesrs1064793817
hgdprs1064793817
ensemblrs1064793817
gopubmedrs1064793817
geneviewrs1064793817
scholarrs1064793817
googlers1064793817
pharmgkbrs1064793817
gwascentralrs1064793817
openSNPrs1064793817
23andMers1064793817
23andMe allrs1064793817
SNPshotrs1064793817
SNPdbers1064793817
MSV3drs1064793817
GWAS Ctlgrs1064793817
Max Magnitude0
ClinVar
Risk rs1064793817(T;T)
Alt rs1064793817(T;T)
Reference Rs1064793817(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CHEK2
CLNDBN not provided
Reversed 1
HGVS NC_000022.10:g.29130682G>A
CLNSRC
CLNACC RCV000480175.1,