Supriya Ghosh (Editor)

Rs1800532

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Name(s)
  
A218C

Chromosome
  
11

Ensembl
  
Human SNPView

Gene
  
TPH1

Region
  
Intron 7

dbSNP
  
1800532

In genetics, rs1800532 (A218C) is a genetic variant. It is a single nucleotide polymorphism in the TPH1 gene and located in intron 7.

It has been examined in relation to personality traits.

A779C is another SNP in same intron.

References

Rs1800532 Wikipedia


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