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rs3732783

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs3732783(A;G)
Make rs3732783(G;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position114171942
GeneDRD3
is asnp
is mentioned by
dbSNPrs3732783
dbSNP (classic)rs3732783
ClinGenrs3732783
ebirs3732783
HLIrs3732783
Exacrs3732783
Gnomadrs3732783
Varsomers3732783
LitVarrs3732783
Maprs3732783
PheGenIrs3732783
Biobankrs3732783
1000 genomesrs3732783
hgdprs3732783
ensemblrs3732783
geneviewrs3732783
scholarrs3732783
googlers3732783
pharmgkbrs3732783
gwascentralrs3732783
openSNPrs3732783
23andMers3732783
SNPshotrs3732783
SNPdbers3732783
MSV3drs3732783
GWAS Ctlgrs3732783
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 24556642OA-icon.png]
Trait Smooth-surface caries
Title Genome-wide association study of primary dentition pit-and-fissure and smooth surface caries.
Risk Allele T
P-val 9E-6
Odds Ratio 1.88 [NR] unit decrease


ClinVar
Risk rs3732783(G;G)
Alt rs3732783(G;G)
Reference Rs3732783(A;A)
Significance Probable-non-pathogenic
Disease Hereditary Essential Tremor
Variation info
Gene DRD3
CLNDBN Hereditary Essential Tremor
Reversed 1
HGVS NC_000003.11:g.113890789T>C
CLNSRC
CLNACC RCV000327367.1,