DisGeNET - a database of gene-disease associations

List of shared variants

RDW - Red blood cell distribution width result, C1304746

Disease: Serum total cholesterol measurement

Source: GWASCAT ×

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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
rs1260326	GCKR	0.645	0.600	2	27508073	missense variant	T/C;G	snv	0.63; 4.0E-06	0.68	55
rs964184	ZPR1	0.716	0.440	11	116778201	3 prime UTR variant	G/C	snv		0.82	35
rs4420638	APOC1	0.708	0.520	19	44919689	downstream gene variant	A/G	snv		0.18	30
rs429358	APOE	0.590	0.600	19	44908684	missense variant	T/C	snv	0.14	0.16	26
rs7412	APOE	0.641	0.640	19	44908822	missense variant	C/T	snv	6.2E-02	7.9E-02	20
rs5744680	POLK	0.851	0.120	5	75584065	intron variant	G/A	snv		0.55	18
rs635634		0.882	0.160	9	133279427	upstream gene variant	T/A;C	snv			17
rs2954021		1.000	0.040	8	125469835	intron variant	A/G	snv		0.54	13
rs738409	PNPLA3	0.557	0.720	22	43928847	missense variant	C/G	snv	0.28	0.22	11
rs7775698	HBS1L	1.000	0.080	6	135097497	intron variant	C/T	snv		6.9E-02	11
rs77542162	ABCA6	1.000	0.040	17	69085137	missense variant	A/G	snv	9.3E-03	1.0E-02	10
rs738408	PNPLA3	0.925	0.120	22	43928850	synonymous variant	C/T	snv	0.28	0.22	9
rs3747207	PNPLA3			22	43928975	intron variant	G/A	snv		0.22	7
rs1042034	APOB	0.851	0.240	2	21002409	missense variant	C/T	snv	0.70	0.78	6
rs55709272	IL1RN			2	113109711	intron variant	T/A;C	snv			5
rs77960347	LIPG			18	49583585	missense variant	A/C;G	snv	4.0E-06; 8.7E-03		5
rs9411378	ABO			9	133270015	intron variant	A/C;T	snv			5
rs586178	RHCE			1	25420739	missense variant	G/A;C	snv	8.4E-05; 0.41		4