DisGeNET - a database of gene-disease associations

Source: GWASDB

Variants associated to the Disease: Protein C antigen measurement ×

Variants associated to the Gene: UQCC1 ×

Results per page

Gene

Disease

Variant

Source

DSI _v

DPI _v

pLI

Consequence

AF_EXOME

AF_GENOME

Variant	Gene	DSI _v	DPI _v	Chr	Position	Consequence	Alleles	Class	AF EXOME	AF GENOME	Num. diseases
rs1570002	UQCC1			20	35328993	intron variant	G/A	snv		5.8E-02	2
rs17092565	UQCC1			20	35326442	intron variant	T/G	snv		8.3E-02	2
rs17092579	UQCC1			20	35330429	intron variant	A/G	snv		6.8E-02	2
rs17331061	UQCC1			20	35375371	intron variant	T/G	snv		4.6E-02	2
rs3764732	UQCC1			20	35303201	3 prime UTR variant	G/A	snv		8.1E-02	2
rs4911488	UQCC1			20	35318770	intron variant	C/G	snv		8.2E-02	2
rs4911489	UQCC1			20	35329284	intron variant	C/T	snv		8.3E-02	2
rs4911495	UQCC1			20	35384175	intron variant	A/C	snv	8.5E-02	6.1E-02	2
rs6058227	UQCC1			20	35308144	intron variant	C/T	snv		0.15	2
rs6060375	UQCC1			20	35333172	intron variant	T/C;G	snv			2
rs6120904	UQCC1			20	35325488	intron variant	G/A;C	snv			2
rs6579229	UQCC1			20	35309781	intron variant	C/A;T	snv			2