rs155100
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;T) | 0 | common in complete genomics |
Make rs155100(A;A) |
Make rs155100(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 181485360 |
Gene | ITGA4 |
is a | snp |
is | mentioned by |
dbSNP | rs155100 |
dbSNP (classic) | rs155100 |
ClinGen | rs155100 |
ebi | rs155100 |
HLI | rs155100 |
Exac | rs155100 |
Gnomad | rs155100 |
Varsome | rs155100 |
LitVar | rs155100 |
Map | rs155100 |
PheGenI | rs155100 |
Biobank | rs155100 |
1000 genomes | rs155100 |
hgdp | rs155100 |
ensembl | rs155100 |
geneview | rs155100 |
scholar | rs155100 |
rs155100 | |
pharmgkb | rs155100 |
gwascentral | rs155100 |
openSNP | rs155100 |
23andMe | rs155100 |
SNPshot | rs155100 |
SNPdbe | rs155100 |
MSV3d | rs155100 |
GWAS Ctlg | rs155100 |
GMAF | 0.4229 |
Max Magnitude | 0 |
? | (A;A) (A;T) (T;T) | 28 |
---|---|---|
|
[PMID 19259978] Association of the alpha4 integrin subunit gene (ITGA4) with autism
[PMID 14681825] Mutation of CERKL, a novel human ceramide kinase gene, causes autosomal recessive retinitis pigmentosa (RP26).
[PMID 18806881] Identification of candidate regions for a novel Usher syndrome type II locus.