DisGeNET - a database of gene-disease associations

Source: GWASDB

Variants associated to the Gene: SMAD3 ×

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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
rs17293632	SMAD3	0.763	0.240	15	67150258	intron variant	C/T	snv		0.17	3
rs744910	SMAD3	1.000	0.080	15	67154447	intron variant	G/A;T	snv			1
rs17228212	SMAD3	0.807	0.160	15	67166301	intron variant	T/C	snv		0.21	1
rs35874463	SMAD3	0.827	0.120	15	67165360	missense variant	A/G	snv	4.0E-02	3.4E-02	1
rs12913547	SMAD3			15	67175169	intron variant	T/C;G	snv			1
rs7181556	SMAD3			15	67184430	intron variant	C/G;T	snv			1
rs4562997	SMAD3			15	67165814	intron variant	G/A;T	snv			1
rs16950687	SMAD3			15	67171675	intron variant	A/G;T	snv			1
rs1866316	SMAD3			15	67149659	intron variant	T/C	snv		0.36	1
rs17294280	SMAD3	0.882	0.120	15	67175947	intron variant	A/G	snv		0.19	1
rs7174445	SMAD3			15	67158877	intron variant	C/G	snv		0.36	1
rs2033784	SMAD3	1.000	0.080	15	67157322	intron variant	A/G	snv		0.35	1
rs17228058	SMAD3	1.000	0.040	15	67157967	intron variant	A/G	snv		0.17	1
rs2278546	SMAD3			15	67174264	intron variant	A/G	snv		0.34	1
rs7173698	SMAD3			15	67158555	intron variant	A/G	snv		0.36	1
rs8032739	SMAD3			15	67156561	intron variant	A/G	snv		0.36	1