rs1077989
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1077989(A;A) |
Make rs1077989(A;C) |
Make rs1077989(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 14 |
Position | 67509105 |
Gene | GPHN, TMEM229B |
is a | snp |
is | mentioned by |
dbSNP | rs1077989 |
dbSNP (classic) | rs1077989 |
ClinGen | rs1077989 |
ebi | rs1077989 |
HLI | rs1077989 |
Exac | rs1077989 |
Gnomad | rs1077989 |
Varsome | rs1077989 |
LitVar | rs1077989 |
Map | rs1077989 |
PheGenI | rs1077989 |
Biobank | rs1077989 |
1000 genomes | rs1077989 |
hgdp | rs1077989 |
ensembl | rs1077989 |
geneview | rs1077989 |
scholar | rs1077989 |
rs1077989 | |
pharmgkb | rs1077989 |
gwascentral | rs1077989 |
openSNP | rs1077989 |
23andMe | rs1077989 |
SNPshot | rs1077989 |
SNPdbe | rs1077989 |
MSV3d | rs1077989 |
GWAS Ctlg | rs1077989 |
GMAF | 0.3838 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22359512] |
Trait | |
Title | Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations. |
Risk Allele | |
P-val | 9E-18 |
Odds Ratio | 0 None |