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rs1057519438

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519438(A;A)
Make rs1057519438(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position87969919
GeneCDK20
is asnp
is mentioned by
dbSNPrs1057519438
dbSNP (classic)rs1057519438
ClinGenrs1057519438
ebirs1057519438
HLIrs1057519438
Exacrs1057519438
Gnomadrs1057519438
Varsomers1057519438
LitVarrs1057519438
Maprs1057519438
PheGenIrs1057519438
Biobankrs1057519438
1000 genomesrs1057519438
hgdprs1057519438
ensemblrs1057519438
geneviewrs1057519438
scholarrs1057519438
googlers1057519438
pharmgkbrs1057519438
gwascentralrs1057519438
openSNPrs1057519438
23andMers1057519438
23andMe allrs1057519438
SNPshotrs1057519438
SNPdbers1057519438
MSV3drs1057519438
GWAS Ctlgrs1057519438
Max Magnitude0
ClinVar
Risk rs1057519438(A;A)
Alt rs1057519438(A;A)
Reference Rs1057519438(G;G)
Significance Pathogenic
Disease Attention deficit hyperactivity disorder Hearing impairment Obsessive-compulsive behavior Seizures
Variation info
Gene CDK20
CLNDBN Attention deficit hyperactivity disorder Hearing impairment Obsessive-compulsive behavior Seizures
Reversed 1
HGVS NC_000009.11:g.90584834C>T
CLNSRC
CLNACC RCV000416444.1,