rs6027755
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6027755(A;A) |
Make rs6027755(A;G) |
Make rs6027755(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 20 |
Position | 60693652 |
is a | snp |
is | mentioned by |
dbSNP | rs6027755 |
dbSNP (classic) | rs6027755 |
ClinGen | rs6027755 |
ebi | rs6027755 |
HLI | rs6027755 |
Exac | rs6027755 |
Gnomad | rs6027755 |
Varsome | rs6027755 |
LitVar | rs6027755 |
Map | rs6027755 |
PheGenI | rs6027755 |
Biobank | rs6027755 |
1000 genomes | rs6027755 |
hgdp | rs6027755 |
ensembl | rs6027755 |
geneview | rs6027755 |
scholar | rs6027755 |
rs6027755 | |
pharmgkb | rs6027755 |
gwascentral | rs6027755 |
openSNP | rs6027755 |
23andMe | rs6027755 |
SNPshot | rs6027755 |
SNPdbe | rs6027755 |
MSV3d | rs6027755 |
GWAS Ctlg | rs6027755 |
GMAF | 0.3136 |
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 | 0.000006 |
Odds Ratio | 1.09 [NR] unit increase |