DisGeNET - a database of gene-disease associations

List of shared variants

Smoking, C0037369

Disease: Height

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
rs6570507	ADGRG6	0.827	0.240	6	142358435	intron variant	G/A	snv		0.47	13
rs3791679	EFEMP1 ; LOC112268416	0.925	0.120	2	55869757	intron variant	A/G	snv		0.20	11
rs1812175	HHIP-AS1 ; HHIP			4	144653692	intron variant	A/G	snv		0.79	6
rs11205277		1.000	0.120	1	149920979	upstream gene variant	A/C;G;T	snv			5
rs2274432	TSEN15			1	184051811	missense variant	G/A	snv	0.33	0.28	5
rs1344674	ZBTB38			3	141406344	intron variant	A/G	snv		0.55	4
rs1776897				6	34227234	regulatory region variant	G/T	snv		0.80	4
rs2638953	CCDC91			12	28381482	intron variant	G/C;T	snv			4
rs3760318	ADAP2			17	30920697	intron variant	G/A	snv		0.39	4
rs473902	PTCH1			9	95493953	intron variant	T/G	snv		5.7E-02	4
rs7697556				4	72649596	intergenic variant	T/A;C	snv			4