DisGeNET - a database of gene-disease associations

Source: GWASDB

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
rs10119	TOMM40	0.925	0.080	19	44903416	3 prime UTR variant	G/A	snv		0.28	3
rs157582	TOMM40	0.851	0.160	19	44892962	intron variant	C/T	snv	0.24	0.29	3
rs34404554	TOMM40	1.000	0.080	19	44892652	intron variant	C/G	snv		0.12	2
rs11556505	TOMM40	0.925	0.080	19	44892887	synonymous variant	C/T	snv	0.13	0.13	2
rs741780	TOMM40	1.000	0.080	19	44901174	intron variant	T/C	snv	0.47	0.52	1
rs760136	TOMM40	1.000	0.080	19	44900601	intron variant	A/G	snv		0.52	1
rs1038026	TOMM40	1.000	0.080	19	44901805	3 prime UTR variant	A/G;T	snv			1
rs1038025	TOMM40	1.000	0.080	19	44901715	3 prime UTR variant	T/C;G	snv			1
rs157590	TOMM40	0.882	0.160	19	44895459	intron variant	A/C	snv		0.60	1
rs405697	TOMM40	1.000	0.080	19	44901434	3 prime UTR variant	A/G;T	snv			1
rs157581	TOMM40	0.925	0.080	19	44892457	synonymous variant	T/C	snv	0.25	0.29	1
rs11668327	TOMM40	1.000	0.080	19	44895376	intron variant	G/C	snv		0.12	1
rs61679753	TOMM40	1.000	0.080	19	44897490	intron variant	T/A	snv		5.6E-02	1
rs76366838	TOMM40			19	44896639	intron variant	G/A;T	snv			1