MIA, MIA SH3 domain containing, 8190

N. diseases: 130; N. variants: 3
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2233152
rs2233152
Entrez Id: 8190;100529262
Gene Symbol: MIA;MIA-RAB4B
MIA;MIA-RAB4B
CUI: C0026691
Disease:
Mucocutaneous Lymph Node Syndrome 		A 0.800 GeneticVariation GWASCAT A genome-wide association study identifies three new risk loci for Kawasaki disease. 22446962 2012
dbSNP: rs2233152
rs2233152
Entrez Id: 8190;100529262
Gene Symbol: MIA;MIA-RAB4B
MIA;MIA-RAB4B
CUI: C0026691
Disease:
Mucocutaneous Lymph Node Syndrome 		A 0.800 GeneticVariation GWASDB A genome-wide association study identifies three new risk loci for Kawasaki disease. 22446962 2012
dbSNP: rs2233154
rs2233154
Entrez Id: 8190;100529262
Gene Symbol: MIA;MIA-RAB4B
MIA;MIA-RAB4B
CUI: C2985280
Disease:
Blood Protein Measurement 		C 0.700 GeneticVariation GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
dbSNP: rs771011224
rs771011224
Entrez Id: 8190;53916;100529262;100529264
Gene Symbol: MIA;RAB4B;MIA-RAB4B;RAB4B-EGLN2
MIA;RAB4B;MIA-RAB4B;RAB4B-EGLN2
CUI: C1306459
Disease:
Primary malignant neoplasm 		0.010 GeneticVariation BEFREE T34A-C84A-dNSur-His is also a potential therapeutic agent for augmenting cancer therapy. 31004782 2019
dbSNP: rs771011224
rs771011224
Entrez Id: 8190;53916;100529262;100529264
Gene Symbol: MIA;RAB4B;MIA-RAB4B;RAB4B-EGLN2
MIA;RAB4B;MIA-RAB4B;RAB4B-EGLN2
CUI: C0006826
Disease:
Malignant Neoplasms 		0.010 GeneticVariation BEFREE T34A-C84A-dNSur-His is also a potential therapeutic agent for augmenting cancer therapy. 31004782 2019