PCDHA11, protocadherin alpha 11, 56138

N. diseases: 4; N. variants: 6
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs190175998
rs190175998
Entrez Id: 9752;56135;56136;56137;56138;56139;56140;56141;56142;56143;56144;56145;56146;56147
Gene Symbol: PCDHA9;PCDHAC1;PCDHA13;PCDHA12;PCDHA11;PCDHA10;PCDHA8;PCDHA7;PCDHA6;PCDHA5;PCDHA4;PCDHA3;PCDHA2;PCDHA1
PCDHA9;PCDHAC1;PCDHA13;PCDHA12;PCDHA11;PCDHA10;PCDHA8;PCDHA7;PCDHA6;PCDHA5;PCDHA4;PCDHA3;PCDHA2;PCDHA1
CUI: C0042834
Disease:
Vital capacity 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs150616068
rs150616068
Entrez Id: 9752;56136;56137;56138;56139;56140;56141;56142;56143;56144;56145;56146;56147
Gene Symbol: PCDHA9;PCDHA13;PCDHA12;PCDHA11;PCDHA10;PCDHA8;PCDHA7;PCDHA6;PCDHA5;PCDHA4;PCDHA3;PCDHA2;PCDHA1
PCDHA9;PCDHA13;PCDHA12;PCDHA11;PCDHA10;PCDHA8;PCDHA7;PCDHA6;PCDHA5;PCDHA4;PCDHA3;PCDHA2;PCDHA1
CUI: C0200641
Disease:
Blood basophil count (lab test) 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs150616068
rs150616068
Entrez Id: 9752;56136;56137;56138;56139;56140;56141;56142;56143;56144;56145;56146;56147
Gene Symbol: PCDHA9;PCDHA13;PCDHA12;PCDHA11;PCDHA10;PCDHA8;PCDHA7;PCDHA6;PCDHA5;PCDHA4;PCDHA3;PCDHA2;PCDHA1
PCDHA9;PCDHA13;PCDHA12;PCDHA11;PCDHA10;PCDHA8;PCDHA7;PCDHA6;PCDHA5;PCDHA4;PCDHA3;PCDHA2;PCDHA1
CUI: C0200633
Disease:
Neutrophil count (procedure) 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs155806
rs155806
Entrez Id: 9752;56134;56135;56136;56137;56138;56139;56140;56141;56142;56143;56144;56145;56146;56147
Gene Symbol: PCDHA9;PCDHAC2;PCDHAC1;PCDHA13;PCDHA12;PCDHA11;PCDHA10;PCDHA8;PCDHA7;PCDHA6;PCDHA5;PCDHA4;PCDHA3;PCDHA2;PCDHA1
PCDHA9;PCDHAC2;PCDHAC1;PCDHA13;PCDHA12;PCDHA11;PCDHA10;PCDHA8;PCDHA7;PCDHA6;PCDHA5;PCDHA4;PCDHA3;PCDHA2;PCDHA1
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs1119032
rs1119032
Entrez Id: 9752;56136;56137;56138;56139;56140;56141;56142;56143;56144;56145;56146;56147
Gene Symbol: PCDHA9;PCDHA13;PCDHA12;PCDHA11;PCDHA10;PCDHA8;PCDHA7;PCDHA6;PCDHA5;PCDHA4;PCDHA3;PCDHA2;PCDHA1
PCDHA9;PCDHA13;PCDHA12;PCDHA11;PCDHA10;PCDHA8;PCDHA7;PCDHA6;PCDHA5;PCDHA4;PCDHA3;PCDHA2;PCDHA1
CUI: C0004352
Disease:
Autistic Disorder 		0.010 GeneticVariation BEFREE Haplotypes involving rs1119032 showed very strong associations with autism, withstanding multiple testing corrections. 23031252 2013
dbSNP: rs155806
rs155806
Entrez Id: 9752;56134;56135;56136;56137;56138;56139;56140;56141;56142;56143;56144;56145;56146;56147
Gene Symbol: PCDHA9;PCDHAC2;PCDHAC1;PCDHA13;PCDHA12;PCDHA11;PCDHA10;PCDHA8;PCDHA7;PCDHA6;PCDHA5;PCDHA4;PCDHA3;PCDHA2;PCDHA1
PCDHA9;PCDHAC2;PCDHAC1;PCDHA13;PCDHA12;PCDHA11;PCDHA10;PCDHA8;PCDHA7;PCDHA6;PCDHA5;PCDHA4;PCDHA3;PCDHA2;PCDHA1
CUI: C0004352
Disease:
Autistic Disorder 		0.010 GeneticVariation BEFREE Five SNPs (rs251379, rs1119032, rs17119271, rs155806 and rs17119346) showed significant associations with autism. 23031252 2013
dbSNP: rs17119271
rs17119271
Entrez Id: 9752;56135;56136;56137;56138;56139;56140;56141;56142;56143;56144;56145;56146;56147
Gene Symbol: PCDHA9;PCDHAC1;PCDHA13;PCDHA12;PCDHA11;PCDHA10;PCDHA8;PCDHA7;PCDHA6;PCDHA5;PCDHA4;PCDHA3;PCDHA2;PCDHA1
PCDHA9;PCDHAC1;PCDHA13;PCDHA12;PCDHA11;PCDHA10;PCDHA8;PCDHA7;PCDHA6;PCDHA5;PCDHA4;PCDHA3;PCDHA2;PCDHA1
CUI: C0004352
Disease:
Autistic Disorder 		0.010 GeneticVariation BEFREE Five SNPs (rs251379, rs1119032, rs17119271, rs155806 and rs17119346) showed significant associations with autism. 23031252 2013
dbSNP: rs17119346
rs17119346
Entrez Id: 9752;56134;56135;56136;56137;56138;56139;56140;56141;56142;56143;56144;56145;56146;56147
Gene Symbol: PCDHA9;PCDHAC2;PCDHAC1;PCDHA13;PCDHA12;PCDHA11;PCDHA10;PCDHA8;PCDHA7;PCDHA6;PCDHA5;PCDHA4;PCDHA3;PCDHA2;PCDHA1
PCDHA9;PCDHAC2;PCDHAC1;PCDHA13;PCDHA12;PCDHA11;PCDHA10;PCDHA8;PCDHA7;PCDHA6;PCDHA5;PCDHA4;PCDHA3;PCDHA2;PCDHA1
CUI: C0004352
Disease:
Autistic Disorder 		0.010 GeneticVariation BEFREE Five SNPs (rs251379, rs1119032, rs17119271, rs155806 and rs17119346) showed significant associations with autism. 23031252 2013