rs2073738
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs2073738(A;A) |
Make rs2073738(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 22 |
Position | 19183443 |
Gene | CLTCL1 |
is a | snp |
is | mentioned by |
dbSNP | rs2073738 |
dbSNP (classic) | rs2073738 |
ClinGen | rs2073738 |
ebi | rs2073738 |
HLI | rs2073738 |
Exac | rs2073738 |
Gnomad | rs2073738 |
Varsome | rs2073738 |
LitVar | rs2073738 |
Map | rs2073738 |
PheGenI | rs2073738 |
Biobank | rs2073738 |
1000 genomes | rs2073738 |
hgdp | rs2073738 |
ensembl | rs2073738 |
geneview | rs2073738 |
scholar | rs2073738 |
rs2073738 | |
pharmgkb | rs2073738 |
gwascentral | rs2073738 |
openSNP | rs2073738 |
23andMe | rs2073738 |
SNPshot | rs2073738 |
SNPdbe | rs2073738 |
MSV3d | rs2073738 |
GWAS Ctlg | rs2073738 |
GMAF | 0.008264 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 22511880] Whole-Exome Sequencing and Homozygosity Analysis Implicate Depolarization-Regulated Neuronal Genes in Autism