RNF13, ring finger protein 13, 11342

N. diseases: 33; N. variants: 1
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs41411047
rs41411047
Entrez Id: 11342;389161
Gene Symbol: RNF13;ANKUB1
RNF13;ANKUB1
CUI: C0027051
Disease:
Myocardial Infarction 		A 0.710 GeneticVariation GWASCAT Several SNPs, including the rs7421388 (PLCL1) and rs12541758 (TRPA1) displaying a suggestive GWAS association (P < 1 × 10(-5)) with CAD as well as rs41411047 (RNF13), rs32793 (PDZD2) and rs4739066 (YTHDF3), similarly showing weak association with MI, were confirmed in an independent dataset. 26708285 2016
dbSNP: rs41411047
rs41411047
Entrez Id: 11342;389161
Gene Symbol: RNF13;ANKUB1
RNF13;ANKUB1
CUI: C0027051
Disease:
Myocardial Infarction 		0.710 GeneticVariation BEFREE Several SNPs, including the rs7421388 (PLCL1) and rs12541758 (TRPA1) displaying a suggestive GWAS association (P < 1 × 10(-5)) with CAD as well as rs41411047 (RNF13), rs32793 (PDZD2) and rs4739066 (YTHDF3), similarly showing weak association with MI, were confirmed in an independent dataset. 26708285 2016
dbSNP: rs41411047
rs41411047
Entrez Id: 11342;389161
Gene Symbol: RNF13;ANKUB1
RNF13;ANKUB1
CUI: C1956346
Disease:
Coronary Artery Disease 		0.010 GeneticVariation BEFREE Several SNPs, including the rs7421388 (PLCL1) and rs12541758 (TRPA1) displaying a suggestive GWAS association (P < 1 × 10(-5)) with CAD as well as rs41411047 (RNF13), rs32793 (PDZD2) and rs4739066 (YTHDF3), similarly showing weak association with MI, were confirmed in an independent dataset. 26708285 2016