Promethease 0.1.82
Rs1047286
From SNPedia
| is a | snp |
| is | mentioned by |
| dbSNP | rs1047286 |
| hapmap | rs1047286 |
| hgdp | rs1047286 |
| ensembl | rs1047286 |
| gopubmed | rs1047286 |
| scholar | rs1047286 |
| rs1047286 | |
| pharmgkb | rs1047286 |
| hgvbaseg2p | rs1047286 |
| medrefsnp | rs1047286 |
| 23andMe | rs1047286 |
| SNP Nexus |
| Gene | C3 |
| Chromosome | 19 |
| Orientation | minus |
| Position | 6664262 |
| Genotype | Effect |
|---|---|
| rs1047286(C;C)* | ? |
| rs1047286(C;T)* | ? |
| rs1047286(T;T)* | ? |
- related to C3 POLYMORPHISM, HAV 4-1 PLUS/MINUS TYPE according to omim 120700.0002
| Neighbor | rs2230199 |
| Distance | 5125 |
| Neighbor | rs2230201 |
| Distance | 29 |
[PMID 19399715] Impact of interacting functional variants in COMT on regional gray matter volume in human brain
[PMID 19234341] Complement component 3 (C3) haplotypes and risk of advanced age-related macular degeneration
[PMID 19850835] The noncoding variant in complement factor H gene increases risk of exudative age-related macular degeneration in a Chinese population
