DisGeNET - a database of gene-disease associations

List of shared variants

Smoking, C0037369

Disease: Intelligence

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
rs13107325	SLC39A8	0.776	0.520	4	102267552	missense variant	C/A;T	snv	4.0E-06; 4.5E-02		34
rs3817334	MTCH2	1.000	0.080	11	47629441	intron variant	C/T	snv		0.36	7
rs3101336	LOC105378797	1.000	0.080	1	72285502	intron variant	T/C	snv		0.62	6
rs2650492	SBK1			16	28322090	3 prime UTR variant	G/A	snv		0.20	5
rs12489828	NT5DC2			3	52532998	intron variant	G/T	snv		0.51	4
rs6012558				20	48914749	intergenic variant	G/A	snv		0.42	4
rs4664442	SLC4A10	1.000	0.040	2	161971491	intron variant	G/A;C	snv			3
rs35891966	NAV2			11	20107765	missense variant	G/A	snv	4.5E-02	4.5E-02	2
rs76608582	HDGFL2			19	4474728	intron variant	C/A;T	snv			2