SNX16, sorting nexin 16, 64089

N. diseases: 2; N. variants: 2
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2600605
rs2600605
Entrez Id: 64089;100128836
Gene Symbol: SNX16;HNRNPA1P36
SNX16;HNRNPA1P36
CUI: C0018498
Disease:
Hair Color 		A 0.700 GeneticVariation GWASCAT Genome-wide study of hair colour in UK Biobank explains most of the SNP heritability. 30531825 2018
dbSNP: rs7833790
rs7833790
Entrez Id: 64089
Gene Symbol: SNX16
SNX16
CUI: C0428883
Disease:
Diastolic blood pressure 		C 0.700 GeneticVariation GWASCAT Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk. 28135244 2017