rs3732783
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs3732783(A;G) |
Make rs3732783(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 3 |
Position | 114171942 |
Gene | DRD3 |
is a | snp |
is | mentioned by |
dbSNP | rs3732783 |
dbSNP (classic) | rs3732783 |
ClinGen | rs3732783 |
ebi | rs3732783 |
HLI | rs3732783 |
Exac | rs3732783 |
Gnomad | rs3732783 |
Varsome | rs3732783 |
LitVar | rs3732783 |
Map | rs3732783 |
PheGenI | rs3732783 |
Biobank | rs3732783 |
1000 genomes | rs3732783 |
hgdp | rs3732783 |
ensembl | rs3732783 |
geneview | rs3732783 |
scholar | rs3732783 |
rs3732783 | |
pharmgkb | rs3732783 |
gwascentral | rs3732783 |
openSNP | rs3732783 |
23andMe | rs3732783 |
SNPshot | rs3732783 |
SNPdbe | rs3732783 |
MSV3d | rs3732783 |
GWAS Ctlg | rs3732783 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 24556642] |
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, |