DisGeNET - a database of gene-disease associations

List of shared variants

Long QT Syndrome, C0023976

Disease: Atrial Fibrillation

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
rs1805123	KCNH2	0.724	0.280	7	150948446	missense variant	T/A;C;G	snv	1.3E-05; 0.18; 8.4E-06		18
rs1805127	KCNE1	0.732	0.240	21	34449523	missense variant	T/C	snv	0.64	2.0E-04	17
rs767910122	KCNH2	0.724	0.280	7	150948446	frameshift variant	-/GTCCG	ins		4.4E-05	17
rs794728448	KCNH2	0.724	0.280	7	150948445	frameshift variant	CT/G	delins			17
rs41261344	SCN5A	0.763	0.120	3	38575385	missense variant	C/T	snv	5.4E-03	2.2E-03	11
rs120074192	KCNQ1	0.763	0.120	11	2527959	missense variant	A/G	snv			10
rs1805128	KCNE1	0.776	0.160	21	34449382	missense variant	C/T	snv	9.4E-03		10
rs199472709	KCNQ1	0.790	0.120	11	2572021	missense variant	G/A;T	snv			7
rs121434500	SNTA1	0.851	0.120	20	33410203	missense variant	G/A	snv	2.0E-05	1.4E-05	5
rs199472687	KCNQ1	0.827	0.120	11	2527962	missense variant	G/A	snv			5
rs121912507	KCNH2	0.882	0.120	7	150951511	missense variant	C/G;T	snv			4