DisGeNET - a database of gene-disease associations

List of shared variants

Triglycerides measurement, C0202236

Disease: Kidney Failure, Chronic

Source: ALL

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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
rs1260326	GCKR	0.645	0.600	2	27508073	missense variant	T/C;G	snv	0.63; 4.0E-06	0.68	81
rs1535	FADS2	0.752	0.240	11	61830500	intron variant	A/G	snv		0.31	24
rs174537	TMEM258 ; MYRF	0.708	0.400	11	61785208	non coding transcript exon variant	G/T	snv		0.28	23
rs102275	TMEM258	0.827	0.320	11	61790331	non coding transcript exon variant	T/C	snv		0.47	18
rs174548	FADS2 ; FADS1	0.851	0.160	11	61803876	5 prime UTR variant	C/G;T	snv			17
rs174583	FADS2	0.807	0.320	11	61842278	intron variant	C/T	snv		0.35	16
rs174576	FADS2	0.851	0.200	11	61836038	intron variant	C/A;T	snv			14
rs174566	FADS1 ; FADS2	0.925	0.160	11	61824890	intron variant	A/G	snv		0.34	8
rs174554	FADS1 ; FADS2	1.000	0.080	11	61811991	intron variant	A/G	snv	0.40	0.28	7
rs174564	FADS2 ; FADS1	1.000	0.080	11	61820833	intron variant	A/G	snv		0.30	4
rs174592	FADS2	1.000	0.080	11	61851136	intron variant	A/G	snv		0.44	4