iUUCD 2.0 - integrated annotations for ubiquitin and ubiquitin-like conjugation database

Disease associated variation - GWASdb
Chr	Pos	SNP ID(dbSNP 142)	Ref	Alt	Ori SNP ID	P-value	Drug Name	Drug Anno	GWAS Trait	HPO ID	DO ID	AA	Type	Trait or Drug
2	172549630	rs6757773	T	A,C	rs6757773	2.50E-04			Suicide attempts in bipolar disorder	HPOID:0007302	DOID:3312	T	intron	GWASdb_trait
2	172558172	rs2138348	G	T	rs2138348	2.49E-04			Suicide attempts in bipolar disorder	HPOID:0007302	DOID:3312	C	intron	GWASdb_trait
2	172560729	rs12185567	A	C	rs12185567	2.49E-04			Suicide attempts in bipolar disorder	HPOID:0007302	DOID:3312	C	intron	GWASdb_trait
2	172563922	rs312925	G	A	rs312925	2.49E-04			Suicide attempts in bipolar disorder	HPOID:0007302	DOID:3312	C	intron	GWASdb_trait
2	172564021	rs312924	A	T	rs312924	2.49E-04			Suicide attempts in bipolar disorder	HPOID:0007302	DOID:3312	T	intron	GWASdb_trait
2	172569587	rs312918	G	C	rs312918	2.51E-04			Suicide attempts in bipolar disorder	HPOID:0007302	DOID:3312	G	intron	GWASdb_trait
2	172576011	rs17427473	A	G	rs17427473	5.32E-04			Nicotine dependence	HPOID:0000707	DOID:0050742	A	intron	GWASdb_trait
2	172577116	rs7597387	T	C	rs7597387	2.66E-04			Suicide attempts in bipolar disorder	HPOID:0007302	DOID:3312	C	intron	GWASdb_trait
2	172577276	rs10206062	A	T	rs10206062	2.68E-04			Suicide attempts in bipolar disorder	HPOID:0007302	DOID:3312	A	intron	GWASdb_trait
2	172579954	rs973889	A	G	rs973889	2.74E-04			Suicide attempts in bipolar disorder	HPOID:0007302	DOID:3312	A	intron	GWASdb_trait
2	172585885	rs10207085	T	G	rs10207085	2.76E-04			Suicide attempts in bipolar disorder	HPOID:0007302	DOID:3312	T	intron	GWASdb_trait
2	172586651	rs2292815	C	G	rs2292815	2.80E-04			Suicide attempts in bipolar disorder	HPOID:0007302	DOID:3312	C	intron	GWASdb_trait
2	172591963	rs6722757	A	G	rs6722757	2.96E-04			Suicide attempts in bipolar disorder	HPOID:0007302	DOID:3312	A	intron	GWASdb_trait
2	172596078	rs6710698	G	C	rs6710698	4.99E-04			Suicide attempts in bipolar disorder	HPOID:0007302	DOID:3312	C	intron	GWASdb_trait

Disease associated variation - OMIM
Ensembl_gene_ID	Approved Gene Symbol	MIM Number
ENSG00000077380.15	DYNC1I2	603331