RPS24, ribosomal protein S24, 6229

N. diseases: 42; N. variants: 9
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7090135
rs7090135
Entrez Id: 6229
Gene Symbol: RPS24
RPS24
CUI: C1837461
Disease:
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
dbSNP: rs7090135
rs7090135
Entrez Id: 6229
Gene Symbol: RPS24
RPS24
CUI: C0410702
Disease:
Adolescent idiopathic scoliosis 		0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
dbSNP: rs16935567
rs16935567
Entrez Id: 6229
Gene Symbol: RPS24
RPS24
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		G 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs1863900
rs1863900
Entrez Id: 6229
Gene Symbol: RPS24
RPS24
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		A 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs7090135
rs7090135
Entrez Id: 6229
Gene Symbol: RPS24
RPS24
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		G 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs7899453
rs7899453
Entrez Id: 6229
Gene Symbol: RPS24
RPS24
CUI: C0428472
Disease:
Serum HDL cholesterol measurement 		0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs7899453
rs7899453
Entrez Id: 6229
Gene Symbol: RPS24
RPS24
CUI: C0392885
Disease:
High density lipoprotein measurement 		0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs886039545
rs886039545
Entrez Id: 6229
Gene Symbol: RPS24
RPS24
CUI: C1260899
Disease:
Anemia, Diamond-Blackfan 		G 0.700 CausalMutation CLINVAR Ribosomal protein S19 and S24 insufficiency cause distinct cell cycle defects in Diamond-Blackfan anemia. 19689926 2009
dbSNP: rs104894189
rs104894189
Entrez Id: 6229
Gene Symbol: RPS24
RPS24
CUI: C1260899
Disease:
Anemia, Diamond-Blackfan 		T 0.700 CausalMutation CLINVAR Ribosomal protein S24 gene is mutated in Diamond-Blackfan anemia. 17186470 2006
dbSNP: rs104894188
rs104894188
Entrez Id: 6229
Gene Symbol: RPS24
RPS24
CUI: C1857719
Disease:
Anemia, Diamond-Blackfan, 3 		T 0.700 CausalMutation CLINVAR
dbSNP: rs104894188
rs104894188
Entrez Id: 6229
Gene Symbol: RPS24
RPS24
CUI: C1260899
Disease:
Anemia, Diamond-Blackfan 		T 0.700 CausalMutation CLINVAR
dbSNP: rs104894189
rs104894189
Entrez Id: 6229
Gene Symbol: RPS24
RPS24
CUI: C1857719
Disease:
Anemia, Diamond-Blackfan, 3 		T 0.700 CausalMutation CLINVAR
dbSNP: rs116840806
rs116840806
Entrez Id: 6229
Gene Symbol: RPS24
RPS24
CUI: C1857719
Disease:
Anemia, Diamond-Blackfan, 3 		TACGGATAG 0.700 CausalMutation CLINVAR
dbSNP: rs116840806
rs116840806
Entrez Id: 6229
Gene Symbol: RPS24
RPS24
CUI: C1260899
Disease:
Anemia, Diamond-Blackfan 		TACGGATAG 0.700 CausalMutation CLINVAR
dbSNP: rs1554841994
rs1554841994
Entrez Id: 6229
Gene Symbol: RPS24
RPS24
CUI: C1260899
Disease:
Anemia, Diamond-Blackfan 		C 0.700 CausalMutation CLINVAR
dbSNP: rs1554841994
rs1554841994
Entrez Id: 6229
Gene Symbol: RPS24
RPS24
CUI: C1857719
Disease:
Anemia, Diamond-Blackfan, 3 		C 0.700 CausalMutation CLINVAR