Rs10790212
From SNPedia
| is a | snp |
| is | mentioned by |
| dbSNP | rs10790212 |
| hapmap | rs10790212 |
| hgdp | rs10790212 |
| ensembl | rs10790212 |
| gopubmed | rs10790212 |
| scholar | rs10790212 |
| rs10790212 | |
| pharmgkb | rs10790212 |
| hgvbaseg2p | rs10790212 |
| medrefsnp | rs10790212 |
| 23andMe | rs10790212 |
| SNP Nexus |
| Chromosome | 11 |
| Orientation | plus |
| Position | 117207899 |
| Genotype | Effect |
|---|---|
| rs10790212(C;C)* | ? |
| rs10790212(C;T)* | ? |
| rs10790212(T;T)* | ? |
[PMID 17357072] associated with schizophrenia rs10790212-rs4938445-rs497768
| ? | (C;C) (C;T) (T;T) |
|---|---|
|
| |
Related to SCHIZOPHRENIA 2; SCZD2
according to omim 603342. See also
Related to FXYD DOMAIN-CONTAINING ION TRANSPORT REGULATOR 6; FXYD6
according to omim 606683. See also
