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rs1064796016

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome22
Position28703500
GeneCHEK2
is asnp
is mentioned by
dbSNPrs1064796016
dbSNP (classic)rs1064796016
ClinGenrs1064796016
ebirs1064796016
HLIrs1064796016
Exacrs1064796016
Gnomadrs1064796016
Varsomers1064796016
LitVarrs1064796016
Maprs1064796016
PheGenIrs1064796016
Biobankrs1064796016
1000 genomesrs1064796016
hgdprs1064796016
ensemblrs1064796016
geneviewrs1064796016
scholarrs1064796016
googlers1064796016
pharmgkbrs1064796016
gwascentralrs1064796016
openSNPrs1064796016
23andMers1064796016
23andMe allrs1064796016
SNPshotrs1064796016
SNPdbers1064796016
MSV3drs1064796016
GWAS Ctlgrs1064796016
Max Magnitude0
ClinVar
Risk rs1064796016(C;C)
Alt rs1064796016(C;C)
Reference Rs1064796016(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CHEK2
CLNDBN not provided
Reversed 1
HGVS NC_000022.10:g.29099488C>G
CLNSRC
CLNACC RCV000485985.1,