SH2D2A, SH2 domain containing 2A, 9047

N. diseases: 11; N. variants: 3
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1800601
rs1800601
Entrez Id: 4914;9047
Gene Symbol: NTRK1;SH2D2A
NTRK1;SH2D2A
CUI: C4310768
Disease:
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1800601
rs1800601
Entrez Id: 4914;9047
Gene Symbol: NTRK1;SH2D2A
NTRK1;SH2D2A
CUI: C4014795
Disease:
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1800601
rs1800601
Entrez Id: 4914;9047
Gene Symbol: NTRK1;SH2D2A
NTRK1;SH2D2A
CUI: C0004364
Disease:
Autoimmune Diseases 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1800601
rs1800601
Entrez Id: 4914;9047
Gene Symbol: NTRK1;SH2D2A
NTRK1;SH2D2A
CUI: C3150797
Disease:
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs926103
rs926103
Entrez Id: 4914;9047
Gene Symbol: NTRK1;SH2D2A
NTRK1;SH2D2A
CUI: C0020676
Disease:
Hypothyroidism 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs928391
rs928391
Entrez Id: 9047
Gene Symbol: SH2D2A
SH2D2A
CUI: C0032181
Disease:
Platelet Count measurement 		C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs926103
rs926103
Entrez Id: 4914;9047
Gene Symbol: NTRK1;SH2D2A
NTRK1;SH2D2A
CUI: C0026769
Disease:
Multiple Sclerosis 		0.010 GeneticVariation BEFREE The GA(16)-rs926103()A haplotype was associated with MS in Norwegians (OR 1.4, P=0.04). 18554728 2008