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rs1064793780

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome22
Position28725242
GeneCHEK2
is asnp
is mentioned by
dbSNPrs1064793780
dbSNP (old)rs1064793780
ClinGenrs1064793780
ebirs1064793780
HLIrs1064793780
Exacrs1064793780
Gnomadrs1064793780
Varsomers1064793780
Maprs1064793780
PheGenIrs1064793780
Biobankrs1064793780
1000 genomesrs1064793780
hgdprs1064793780
ensemblrs1064793780
gopubmedrs1064793780
geneviewrs1064793780
scholarrs1064793780
googlers1064793780
pharmgkbrs1064793780
gwascentralrs1064793780
openSNPrs1064793780
23andMers1064793780
23andMe allrs1064793780
SNPshotrs1064793780
SNPdbers1064793780
MSV3drs1064793780
GWAS Ctlgrs1064793780
Max Magnitude0
ClinVar
Risk rs1064793780(-;-)
Alt rs1064793780(-;-)
Reference Rs1064793780(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene CHEK2
CLNDBN not provided
Reversed 1
HGVS NC_000022.10:g.29121230delC
CLNSRC
CLNACC RCV000484271.1,