Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs145406238
rs145406238
Entrez Id: 144717
Gene Symbol: PHETA1
PHETA1
CUI: C0200638
Disease:
Eosinophil count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs3809272
rs3809272
Entrez Id: 144717
Gene Symbol: PHETA1
PHETA1
CUI: C0032181
Disease:
Platelet Count measurement 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs933399
rs933399
Entrez Id: 144717;105369984
Gene Symbol: PHETA1;LINC02356
PHETA1;LINC02356
CUI: C0005586
Disease:
Bipolar Disorder 		0.010 GeneticVariation BEFREE Two SNPs (rs3847953 and rs933399) and an insertion/deletion with putative functional relevance (which are in high LD with each other and with the microsatellite marker) showed significant or nearly significant association with bipolar disorder after Bonferroni-correction (reaching nominal P values from P = 0.002 to P = 0.005). 15389760 2005