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rs10153620

From SNPedia

Orientationplus
Stabilizedplus
Make rs10153620(C;C)
Make rs10153620(C;G)
Make rs10153620(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position205195913
GenePARD3B
is asnp
is mentioned by
dbSNPrs10153620
dbSNP (classic)rs10153620
ClinGenrs10153620
ebirs10153620
HLIrs10153620
Exacrs10153620
Gnomadrs10153620
Varsomers10153620
LitVarrs10153620
Maprs10153620
PheGenIrs10153620
Biobankrs10153620
1000 genomesrs10153620
hgdprs10153620
ensemblrs10153620
geneviewrs10153620
scholarrs10153620
googlers10153620
pharmgkbrs10153620
gwascentralrs10153620
openSNPrs10153620
23andMers10153620
SNPshotrs10153620
SNPdbers10153620
MSV3drs10153620
GWAS Ctlgrs10153620
GMAF0.2727
Max Magnitude0
? (C;C) (C;G) (G;G) 28


GWAS snp
PMID [PMID 23527680]
Trait Attention deficit hyperactivity disorder (combined symptoms)
Title Genome-wide association study of inattention and hyperactivity-impulsivity measured as quantitative traits.
Risk Allele C
P-val 6E-6
Odds Ratio NR NR