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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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
View BVdb publication page