DisGeNET - a database of gene-disease associations

List of associated variants

Serum albumin measurement, C0523465

Source: ALL

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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 GENOME	Num. diseases
rs1883025	ABCA1	0.807	0.120	9	104902020	intron variant	C/T	snv	0.28	13
rs529565	ABO	0.851	0.120	9	133274084	intron variant	C/T	snv		13
rs603424	PKD2L1	1.000	0.080	10	100315722	intron variant	G/A	snv	0.34	13
rs6742078	UGT1A3 ; UGT1A7 ; UGT1A8 ; UGT1A10 ; UGT1A6 ; UGT1A4 ; UGT1A9 ; UGT1A1 ; UGT1A5	0.807	0.240	2	233763993	intron variant	G/T	snv	0.36	13
rs10468017	ALDH1A2	0.851	0.120	15	58386313	intron variant	C/T	snv	0.24	12
rs1532624	CETP	0.851	0.160	16	56971567	intron variant	C/A	snv	0.34	12
rs174570	FADS2	0.882	0.200	11	61829740	intron variant	C/T	snv	0.15	11
rs4148325	UGT1A8 ; UGT1A5 ; UGT1A10 ; UGT1A7 ; UGT1A1 ; UGT1A9 ; UGT1A3 ; UGT1A4 ; UGT1A6	0.851	0.080	2	233764663	intron variant	C/T	snv	0.36	11
rs1864163	CETP	0.882	0.120	16	56963321	intron variant	G/A	snv	0.26	10
rs2068834	ZNF512	0.925	0.120	2	27616672	intron variant	T/C	snv	0.28	10
rs2075290	ZPR1	0.882	0.160	11	116782580	intron variant	C/G;T	snv		10
rs514659	ABO	0.882	0.120	9	133266790	intron variant	C/A;T	snv		10
rs612169	ABO			9	133268030	intron variant	G/A	snv		10
rs6589566	ZPR1	0.882	0.080	11	116781707	intron variant	G/A;C;T	snv		10
rs780092	GCKR	0.827	0.160	2	27520287	intron variant	A/G	snv	0.18	10
rs17145750	MLXIPL	0.925	0.120	7	73612048	intron variant	C/A;T	snv		9
rs17863787	UGT1A9 ; UGT1A8 ; UGT1A6 ; UGT1A7 ; UGT1A10	0.925	0.040	2	233702448	intron variant	T/G	snv	0.30	9
rs2043085	ALDH1A2	0.827	0.080	15	58388755	intron variant	T/C	snv	0.54	9
rs4665972	SNX17			2	27375230	intron variant	T/C	snv	0.69	9
rs929596	UGT1A5 ; UGT1A4 ; UGT1A9 ; UGT1A10 ; UGT1A8 ; UGT1A7 ; UGT1A6 ; UGT1A3 ; UGT1A1	0.925	0.040	2	233765830	intron variant	A/G	snv	0.32	9
rs12721046	APOC1			19	44917997	intron variant	G/A	snv	0.11	8
rs174541	FADS2	1.000	0.080	11	61798436	intron variant	T/C	snv	0.29	8
rs174566	FADS1 ; FADS2	0.925	0.160	11	61824890	intron variant	A/G	snv	0.34	8
rs1748195	DOCK7	0.851	0.120	1	62583922	intron variant	C/G;T	snv		8
rs2678379	APOB	1.000	0.080	2	21003688	intron variant	A/G	snv	0.76	8