Name(s) A779C Chromosome 11 Ensembl Human SNPView | Gene TPH1 Region Intron 7 dbSNP 1799913 | |
In genetics, rs1799913, also called A779C, is a gene variation—a single nucleotide polymorphism (SNP)— in the TPH1 gene. It is located in intron 7.
The SNP association with schizophrenia has been examined in several studies, though as of 2007 with no definitive conclusion.
One study has found that the SNP may be associated with heroin addiction.
A218C (rs1800532) is another SNP in the same intron in the same gene.
References
Rs1799913 Wikipedia(Text) CC BY-SA