DisGeNET - a database of gene-disease associations

List of shared variants

Multiple Sclerosis, C0026769

Disease: Cardiomyopathy, Dilated

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
rs3130000	DHX16	1.000	0.080	6	30660305	non coding transcript exon variant	A/G;T	snv			2
rs4713429	HCG22	1.000	0.080	6	31053240	upstream gene variant	C/G	snv		0.20	2
rs9262615	HCG22	1.000	0.080	6	31053384	upstream gene variant	C/G	snv		0.21	2
rs9262635	HCG22	1.000	0.080	6	31057702	intron variant	A/G	snv		0.22	2
rs9262636	HCG22	1.000	0.080	6	31058071	intron variant	A/G	snv		0.22	2