DisGeNET - a database of gene-disease associations

List of shared variants

Polysomnography, C0162701

Disease: Serum albumin measurement

Source: GWASDB ×

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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 EXOME	AF GENOME	Num. diseases
rs579459		0.752	0.320	9	133278724	upstream gene variant	C/T	snv		0.81	17
rs657152	ABO	0.882	0.200	9	133263862	intron variant	A/C;T	snv			14
rs687289	ABO	1.000	0.120	9	133261703	intron variant	A/G	snv			9
rs10830963	MTNR1B	0.776	0.400	11	92975544	intron variant	C/G	snv		0.22	6
rs662799	APOA5	0.689	0.480	11	116792991	upstream gene variant	G/A	snv		0.90	6
rs3741298	ZPR1			11	116786845	intron variant	C/T	snv		0.73	3
rs1912826	KLKB1			4	186228386	intron variant	G/A;C	snv			2
rs3733402	KLKB1	1.000	0.040	4	186236880	missense variant	G/A;C	snv	0.54		2
rs4253238	KLKB1	0.925	0.080	4	186227233	intron variant	C/T	snv		0.59	2
rs6584202	PYROXD2			10	98410626	non coding transcript exon variant	G/A;C	snv			2