PAH c.912+1452C>T

Variant ID: 12-103244013-G-A

NM_000277.1(PAH):c.912+1452C>T

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Mini-haplotypes as lineage informative SNPs and ancestry inference SNPs.

European Journal Of Human Genetics : Ejhg
Pakstis, Andrew J AJ; Fang, Rixun R; Furtado, Manohar R MR; Kidd, Judith R JR; Kidd, Kenneth K KK
Publication Date: 2012-11

Variant appearance in text: rs869916
PubMed Link: 22535184
Variant Present in the following documents:
  • Main text
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