OLFM2, olfactomedin 2, 93145

N. diseases: 14; N. variants: 7
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1862471
rs1862471
Entrez Id: 93145
Gene Symbol: OLFM2
OLFM2
CUI: C1314691
Disease:
Age at menarche 		0.800 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965 2016
dbSNP: rs1862471
rs1862471
Entrez Id: 93145
Gene Symbol: OLFM2
OLFM2
CUI: C1314691
Disease:
Age at menarche 		G 0.800 GeneticVariation GWASCAT Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. 21102462 2010
dbSNP: rs1862471
rs1862471
Entrez Id: 93145
Gene Symbol: OLFM2
OLFM2
CUI: C1314691
Disease:
Age at menarche 		G 0.800 GeneticVariation GWASDB Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. 21102462 2010
dbSNP: rs4804474
rs4804474
Entrez Id: 93145
Gene Symbol: OLFM2
OLFM2
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs8112411
rs8112411
Entrez Id: 93145
Gene Symbol: OLFM2
OLFM2
CUI: C1314691
Disease:
Age at menarche 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2303100
rs2303100
Entrez Id: 93145
Gene Symbol: OLFM2
OLFM2
CUI: C0424574
Disease:
Duration of sleep 		C 0.700 GeneticVariation GWASCAT GWAS identifies 14 loci for device-measured physical activity and sleep duration. 30531941 2018
dbSNP: rs889122
rs889122
Entrez Id: 93145
Gene Symbol: OLFM2
OLFM2
CUI: C1314691
Disease:
Age at menarche 		G 0.700 GeneticVariation GWASCAT Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche. 25231870 2014
dbSNP: rs1298178636
rs1298178636
Entrez Id: 93145
Gene Symbol: OLFM2
OLFM2
CUI: C0009402
Disease:
Colorectal Carcinoma 		0.700 GeneticVariation UNIPROT
dbSNP: rs779032127
rs779032127
Entrez Id: 93145
Gene Symbol: OLFM2
OLFM2
CUI: C0017612
Disease:
Glaucoma, Open-Angle 		0.010 GeneticVariation BEFREE The Arg144Gln mutation in OLFM2 is a possible disease-causing mutation in Japanese patients with OAG. 17122126 2006