rs1305088
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs1305088(A;A) |
Make rs1305088(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 13 |
Position | 28704313 |
Gene | SLC46A3 |
is a | snp |
is | mentioned by |
dbSNP | rs1305088 |
dbSNP (classic) | rs1305088 |
ClinGen | rs1305088 |
ebi | rs1305088 |
HLI | rs1305088 |
Exac | rs1305088 |
Gnomad | rs1305088 |
Varsome | rs1305088 |
LitVar | rs1305088 |
Map | rs1305088 |
PheGenI | rs1305088 |
Biobank | rs1305088 |
1000 genomes | rs1305088 |
hgdp | rs1305088 |
ensembl | rs1305088 |
geneview | rs1305088 |
scholar | rs1305088 |
rs1305088 | |
pharmgkb | rs1305088 |
gwascentral | rs1305088 |
openSNP | rs1305088 |
23andMe | rs1305088 |
SNPshot | rs1305088 |
SNPdbe | rs1305088 |
MSV3d | rs1305088 |
GWAS Ctlg | rs1305088 |
GMAF | 0.202 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20708005] |
Trait | |
Title | Genome-Wide Association Study Identifies Variants Associated with Histologic Features of Nonalcoholic Fatty Liver Disease |
Risk Allele | A |
P-val | 0.000009 |
Odds Ratio | 0.58 [NR] unit increase |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 13
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d