Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3739821
rs3739821
Entrez Id: 8818;399665
Gene Symbol: DPM2;FAM102A
DPM2;FAM102A
CUI: C0017606
Disease:
Primary angle-closure glaucoma 		0.710 GeneticVariation BEFREE Genotype data of the 8 PACG single-nucleotide polymorphisms (SNPs) (rs11024102 at PLEKHA7, rs3753841 at COL11A1, rs1015213 located between PCMTD1 and ST18 on Chromosome 8q, rs3816415 at EPDR1, rs1258267 at CHAT, rs736893 at GLIS3, rs7494379 at FERMT2, and rs3739821 mapping in between DPM2 and FAM102A) were available. 31377279 2019
dbSNP: rs3739821
rs3739821
Entrez Id: 8818;399665
Gene Symbol: DPM2;FAM102A
DPM2;FAM102A
CUI: C0017606
Disease:
Primary angle-closure glaucoma 		G 0.710 GeneticVariation GWASCAT Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma. 27064256 2016
dbSNP: rs62585312
rs62585312
Entrez Id: 399665
Gene Symbol: FAM102A
FAM102A
CUI: C0202239
Disease:
Uric acid measurement (procedure) 		C 0.700 GeneticVariation GWASCAT Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels. 31578528 2019
dbSNP: rs3739821
rs3739821
Entrez Id: 8818;399665
Gene Symbol: DPM2;FAM102A
DPM2;FAM102A
CUI: C0017605
Disease:
Angle Closure Glaucoma 		0.010 GeneticVariation BEFREE Genotype data of the 8 PACG single-nucleotide polymorphisms (SNPs) (rs11024102 at PLEKHA7, rs3753841 at COL11A1, rs1015213 located between PCMTD1 and ST18 on Chromosome 8q, rs3816415 at EPDR1, rs1258267 at CHAT, rs736893 at GLIS3, rs7494379 at FERMT2, and rs3739821 mapping in between DPM2 and FAM102A) were available. 31377279 2019