rs6079395
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6079395(A;A) |
Make rs6079395(A;G) |
Make rs6079395(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 20 |
Position | 14347253 |
Gene | MACROD2 |
is a | snp |
is | mentioned by |
dbSNP | rs6079395 |
dbSNP (classic) | rs6079395 |
ClinGen | rs6079395 |
ebi | rs6079395 |
HLI | rs6079395 |
Exac | rs6079395 |
Gnomad | rs6079395 |
Varsome | rs6079395 |
LitVar | rs6079395 |
Map | rs6079395 |
PheGenI | rs6079395 |
Biobank | rs6079395 |
1000 genomes | rs6079395 |
hgdp | rs6079395 |
ensembl | rs6079395 |
geneview | rs6079395 |
scholar | rs6079395 |
rs6079395 | |
pharmgkb | rs6079395 |
gwascentral | rs6079395 |
openSNP | rs6079395 |
23andMe | rs6079395 |
SNPshot | rs6079395 |
SNPdbe | rs6079395 |
MSV3d | rs6079395 |
GWAS Ctlg | rs6079395 |
GMAF | 0.404 |
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 | 0.000007 |
Odds Ratio | 0.92 [NR] unit increase |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 20
- 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