Rs1800532

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

Name(s)A218C
RegionIntron 7
Quick facts SNP: rs1800532, Name(s) ...
SNP: rs1800532
Name(s)A218C
GeneTPH1
Chromosome11
RegionIntron 7
External databases
EnsemblHuman SNPView
dbSNP1800532
HapMap1800532
SNPedia1800532
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It has been examined in relation to personality traits.[1][2][3]

A779C is another SNP in same intron.

References

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