DisGeNET - a database of gene-disease associations

List of shared variants

QRS complex feature, C0429097

Disease: QT interval feature (observable entity)

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
rs3825214	TBX5	0.851	0.080	12	114357638	intron variant	G/A	snv		0.77	8
rs6801957	SCN10A	1.000	0.080	3	38725824	intron variant	T/C	snv		0.67	7
rs11708996	SCN5A	0.925	0.120	3	38592432	intron variant	G/C	snv		0.11	6
rs11153730				6	118346359	intergenic variant	T/C	snv		0.40	4
rs11710077	SCN5A			3	38616408	intron variant	A/T	snv		0.17	3
rs12036340				1	162045950	intergenic variant	A/G	snv		0.24	2
rs728926	KLF12			13	73938985	intron variant	C/T	snv		0.34	2