DisGeNET - a database of gene-disease associations

Source: GWASCAT

Variants associated to the Gene: PRTFDC1 ×

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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
rs12266014	PRTFDC1			10	24922362	intron variant	C/T	snv		0.26	7
rs11014285	PRTFDC1			10	24889935	intron variant	G/A	snv		0.11	2
rs10828725	PRTFDC1			10	24929314	intron variant	G/T	snv		0.26	2
rs11818463	PRTFDC1			10	24934438	intron variant	G/A;C	snv			2
rs7905553	PRTFDC1			10	24911662	intron variant	C/G;T	snv			2
rs140884840	PRTFDC1			10	24911877	intron variant	CAAACAAA/-;CAAA	delins			1
rs151165649	PRTFDC1			10	24918312	intron variant	G/A	snv		6.9E-03	1
rs1033962	PRTFDC1	1.000	0.040	10	24927877	intron variant	C/T	snv		0.33	1
rs7394259	PRTFDC1			10	24877899	intron variant	G/A	snv		0.12	1
rs11014271	PRTFDC1			10	24871573	intron variant	C/T	snv		0.12	1
rs10828723	PRTFDC1			10	24916129	intron variant	T/C	snv		0.26	1
rs11014291	PRTFDC1			10	24909758	intron variant	T/C	snv		0.26	1
rs11014296	PRTFDC1			10	24913109	intron variant	C/T	snv		0.26	1