RRAS2, RAS related 2, 22800

N. diseases: 48; N. variants: 4
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11606692
rs11606692
Entrez Id: 22800
Gene Symbol: RRAS2
RRAS2
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2970332
rs2970332
Entrez Id: 22800
Gene Symbol: RRAS2
RRAS2
CUI: C0205682
Disease:
Waist-Hip Ratio 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs182244780
rs182244780
Entrez Id: 22800
Gene Symbol: RRAS2
RRAS2
CUI: C0523979
Disease:
Vitamin D3 measurement 		A 0.700 GeneticVariation GWASCAT Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis. 28757204 2017
dbSNP: rs182244780
rs182244780
Entrez Id: 22800
Gene Symbol: RRAS2
RRAS2
CUI: C0919758
Disease:
Vitamin D measurement 		A 0.700 GeneticVariation GWASCAT Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis. 28757204 2017
dbSNP: rs113954997
rs113954997
Entrez Id: 22800
Gene Symbol: RRAS2
RRAS2
CUI: C0919267
Disease:
ovarian neoplasm 		A 0.700 CausalMutation CLINVAR
dbSNP: rs113954997
rs113954997
Entrez Id: 22800
Gene Symbol: RRAS2
RRAS2
CUI: C4551602
Disease:
Noonan Syndrome 1 		A 0.700 CausalMutation CLINVAR
dbSNP: rs113954997
rs113954997
Entrez Id: 22800
Gene Symbol: RRAS2
RRAS2
CUI: C1140680
Disease:
Malignant neoplasm of ovary 		0.700 GeneticVariation UNIPROT
dbSNP: rs2970332
rs2970332
Entrez Id: 22800
Gene Symbol: RRAS2
RRAS2
CUI: C0030567
Disease:
Parkinson Disease 		0.010 GeneticVariation BEFREE The DCC rs17468382 and EPHB1 rs2030737 SNPs may be associated with increased PD risk, and the CHP rs6492998 and RRAS2 rs2970332 SNPs may be associated with reduced PD risk. 21085126 2011