Rs9550642
From SNPedia
| is a | snp |
| is | mentioned by |
| dbSNP | rs9550642 |
| hapmap | rs9550642 |
| hgdp | rs9550642 |
| ensembl | rs9550642 |
| gopubmed | rs9550642 |
| scholar | rs9550642 |
| rs9550642 | |
| pharmgkb | rs9550642 |
| hgvbaseg2p | rs9550642 |
| medrefsnp | rs9550642 |
| 23andMe | rs9550642 |
| SNP Nexus |
| Gene | LOC100133618 |
| Chromosome | 13 |
| Orientation | plus |
| Position | 19848092 |
| Genotype | Effect |
|---|---|
| rs9550642(A;A) | 2.2x risk |
| rs9550642(A;G) | 1.3x risk |
| rs9550642(G;G) | normal |
| Genotypes | Magnitude | Summary |
|---|---|---|
| Rs9550642(A;A) | 2.2x risk | |
| Rs9550642(A;G) | 1.3x risk | |
| Rs9550642(G;G) | 00 | normal |
The risk allele (oriented to the dbSNP entry) is (A); the odds ratio associated with heterozygotes is 1.34 (CI 1.15-1.56), and for homozygotes, 2.23 (CI 1.21-4.13). [PMID 17554300]
| ? | (A;A) (A;G) (G;G) |
|---|---|
|
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