DisGeNET - a database of gene-disease associations

List of associated variants

P wave duration (observable entity), C0429021

Source: CURATED ×

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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
rs174577	FADS2	1.000	0.080	11	61837342	intron variant	C/A	snv		0.38	12
rs6801957	SCN10A	1.000	0.080	3	38725824	intron variant	T/C	snv		0.67	5
rs452036	MYH6			14	23396676	intron variant	G/A;C	snv	0.33		3
rs6790396	SCN10A	1.000	0.080	3	38730434	intron variant	C/G	snv		0.67	3
rs3922844	SCN5A			3	38582762	intron variant	T/C	snv		0.61	3
rs11689011	EPAS1	1.000	0.120	2	46314037	intron variant	T/A;C;G	snv			2
rs11894252	EPAS1	0.925	0.120	2	46306237	intron variant	T/A;C;G	snv			2
rs2798334	KCND3			1	111894722	intron variant	T/C;G	snv			2
rs41312411	SCN5A			3	38579746	intron variant	C/G	snv		0.11	2
rs1895582	TBX5			12	114369230	intron variant	G/A	snv		0.70	2
rs7312625	TBX5	1.000	0.080	12	114362169	intron variant	G/A	snv		0.71	2
rs1467026				3	12789276	upstream gene variant	G/A	snv		0.67	1
rs4276421				5	45801977	intergenic variant	C/T	snv		0.51	1
rs2285703	CAMK2D			4	113467664	intron variant	A/G	snv		0.21	1
rs13242816	CAV1			7	116549322	intron variant	C/T	snv		7.6E-02	1
rs3801995	CAV1			7	116550543	intron variant	C/T	snv		0.29	1
rs562408	SSBP3			1	54276945	intron variant	A/G	snv		0.61	1
rs148020424	TBX5			12	114367252	intron variant	-/AAAGAAAAGAGAAA;AGAAA	ins			1