DisGeNET - a database of gene-disease associations

Source: GWASDB

Variants associated to the Disease: Serum total cholesterol measurement ×

Variants associated to the Gene: TOMM40 ×

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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
rs2075650	TOMM40	0.662	0.360	19	44892362	intron variant	A/G	snv	0.13	0.13	20
rs157580	TOMM40	0.882	0.160	19	44892009	intron variant	G/A	snv		0.69	11
rs1160985	TOMM40	1.000	0.080	19	44900155	intron variant	C/T	snv		0.52	5
rs8106922	TOMM40	1.000	0.080	19	44898409	intron variant	A/G	snv		0.36	4
rs1038026	TOMM40	1.000	0.080	19	44901805	3 prime UTR variant	A/G;T	snv			1
rs76366838	TOMM40			19	44896639	intron variant	G/A;T	snv			1