TNIP1, TNFAIP3 interacting protein 1, 10318

N. diseases: 93; N. variants: 19
Disease: Myasthenia Gravis ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1422673
rs1422673
Entrez Id: 10318
Gene Symbol: TNIP1
TNIP1
CUI: C0026896
Disease:
Myasthenia Gravis 		0.700 GeneticVariation GWASDB Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08. 23055271 2012
dbSNP: rs2233287
rs2233287
Entrez Id: 10318
Gene Symbol: TNIP1
TNIP1
CUI: C0026896
Disease:
Myasthenia Gravis 		0.700 GeneticVariation GWASDB Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08. 23055271 2012
dbSNP: rs3792783
rs3792783
Entrez Id: 10318
Gene Symbol: TNIP1
TNIP1
CUI: C0026896
Disease:
Myasthenia Gravis 		0.700 GeneticVariation GWASDB Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08. 23055271 2012
dbSNP: rs3792785
rs3792785
Entrez Id: 10318
Gene Symbol: TNIP1
TNIP1
CUI: C0026896
Disease:
Myasthenia Gravis 		0.700 GeneticVariation GWASDB Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08. 23055271 2012
dbSNP: rs4958881
rs4958881
Entrez Id: 10318
Gene Symbol: TNIP1
TNIP1
CUI: C0026896
Disease:
Myasthenia Gravis 		G 0.700 GeneticVariation GWASDB Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08. 23055271 2012