Rs1055061
From SNPedia
| Orientation | minus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1055061 |
| PheGenI | rs1055061 |
| nextbio | rs1055061 |
| hapmap | rs1055061 |
| 1000 genomes | rs1055061 |
| hgdp | rs1055061 |
| ensembl | rs1055061 |
| gopubmed | rs1055061 |
| geneview | rs1055061 |
| scholar | rs1055061 |
| rs1055061 | |
| pharmgkb | rs1055061 |
| gwascentral | rs1055061 |
| openSNP | rs1055061 |
| 23andMe | rs1055061 |
| 23andMe all | rs1055061 |
| SNP Nexus | |
| SNPshot | rs1055061 |
| SNPdbe | rs1055061 |
| MSV3d | rs1055061 |
| Gene | HOMEZ |
| Chromosome | 14 |
| Orientation | minus |
| GMAF | 0.0929 |
| Position | 23744932 |
| Reference | GRCh37 37.1/131 |
| Max Magnitude | 0 |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs1055061(A;A) |
| Make rs1055061(A;G) |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
[PMID 20422016] Consanguinity mapping of congenital heart disease in a South Indian population
| GET Evidence | |
|---|---|
| HOMEZ-R502Q | |
| aa_change | Arg502Gln |
| aa_change_short | R502Q |
| impact | not reviewed |
| qualified_impact | Insufficiently evaluated not reviewed |
| overall_frequency | 0.0940753 |
| summary | |
