DisGeNET - a database of gene-disease associations

Source: GWASCAT

Variants associated to the Gene: TMCC2 ×

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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
rs61823972	TMCC2			1	205232197	intron variant	A/C;T	snv			4
rs896322	LOC101929459 ; TMCC2			1	205240617	intron variant	A/G	snv		0.92	1
rs748012	TMCC2			1	205247445	intron variant	G/A	snv		0.27	1
rs1172128	TMCC2			1	205276105	intron variant	A/G	snv		0.94	1
rs1668871	TMCC2			1	205268009	intron variant	T/C;G	snv			1
rs9660992	TMCC2			1	205280322	intron variant	A/G	snv		0.43	1
rs1172130	TMCC2			1	205275825	intron variant	G/A	snv		0.30	1
rs1172129	TMCC2			1	205275844	intron variant	T/A	snv		0.30	1
rs1668873	TMCC2			1	205266862	intron variant	G/A	snv		0.27	1
rs1151786	TMCC2			1	205258632	intron variant	G/A;C;T	snv			1
rs1172135	TMCC2			1	205278032	non coding transcript exon variant	G/C;T	snv			1
rs1172149	TMCC2			1	205255630	intron variant	A/G	snv		0.51	1