rs4954218
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4954218(G;G) |
| Make rs4954218(G;T) |
| Make rs4954218(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 135045855 |
| Gene | MAP3K19 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4954218 |
| dbSNP (classic) | rs4954218 |
| ClinGen | rs4954218 |
| ebi | rs4954218 |
| HLI | rs4954218 |
| Exac | rs4954218 |
| Gnomad | rs4954218 |
| Varsome | rs4954218 |
| LitVar | rs4954218 |
| Map | rs4954218 |
| PheGenI | rs4954218 |
| Biobank | rs4954218 |
| 1000 genomes | rs4954218 |
| hgdp | rs4954218 |
| ensembl | rs4954218 |
| geneview | rs4954218 |
| scholar | rs4954218 |
| rs4954218 | |
| pharmgkb | rs4954218 |
| gwascentral | rs4954218 |
| openSNP | rs4954218 |
| 23andMe | rs4954218 |
| SNPshot | rs4954218 |
| SNPdbe | rs4954218 |
| MSV3d | rs4954218 |
| GWAS Ctlg | rs4954218 |
| GMAF | 0.0978 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21979947 |
| Trait | |
| Title | A genome-wide association study identifies a potential novel gene locus for keratoconus, one of the commonest causes for corneal transplantation in developed countries. |
| Risk Allele | |
| P-val | 1E-9 |
| Odds Ratio | 1.6100 [NR] |
[PMID 23833071
] Replication and meta-analysis of candidate loci identified variation at RAB3GAP1 associated with keratoconus
[PMID 25675348] Evaluating the Association between Keratoconus and Reported Genetic Loci in a Han Chinese Population
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 2
- 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 NatGeo2
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d
