DisGeNET - a database of gene-disease associations

List of shared variants

Calcification of coronary artery, C1611184

Disease: Pseudocholinesterase Measurement

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 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	81
rs1333049	CDKN2B-AS1	0.614	0.520	9	22125504	intron variant	G/C	snv		0.41	60
rs964184	ZPR1	0.716	0.440	11	116778201	3 prime UTR variant	G/C	snv		0.82	47
rs4977574	CDKN2B-AS1	0.695	0.520	9	22098575	intron variant	A/G;T	snv			26
rs6511720	LDLR	0.790	0.120	19	11091630	intron variant	G/T	snv		0.12	15
rs1532085	ALDH1A2	0.882	0.080	15	58391167	intron variant	A/G;T	snv			13
rs173539		0.882	0.080	16	56954132	intergenic variant	C/T	snv		0.33	11
rs12678919		0.882	0.080	8	19986711	intergenic variant	A/G	snv		1.0E-01	10
rs445925	APOC1	0.882	0.080	19	44912383	non coding transcript exon variant	G/A;C	snv			10