DisGeNET - a database of gene-disease associations

Source: ALL

Variants associated to the Disease: Primary biliary cirrhosis ×

Variants associated to the Gene: TNFRSF1A ×

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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
rs767455	TNFRSF1A	0.742	0.400	12	6341779	synonymous variant	T/C	snv	0.37	0.40	13
rs1800693	TNFRSF1A	0.776	0.360	12	6330843	non coding transcript exon variant	T/C	snv	0.36; 4.0E-06	0.38	9
rs1860545	TNFRSF1A	0.790	0.200	12	6337611	intron variant	G/A	snv		0.31	7
rs4149576	TNFRSF1A	0.882	0.200	12	6339949	intron variant	C/T	snv		0.32	3
rs4149580	TNFRSF1A	1.000	0.080	12	6337824	intron variant	G/A	snv		0.30	1
rs4149581	TNFRSF1A	1.000	0.080	12	6337819	intron variant	T/A;C	snv			1