DisGeNET - a database of gene-disease associations

List of shared variants

Serum albumin measurement, C0523465

Disease: Fasting blood sugar result

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
rs780094	GCKR	0.658	0.400	2	27518370	intron variant	T/C	snv		0.67	62
rs10830963	MTNR1B	0.776	0.400	11	92975544	intron variant	C/G	snv		0.22	27
rs174537	TMEM258 ; MYRF	0.708	0.400	11	61785208	non coding transcript exon variant	G/T	snv		0.28	23
rs560887	SPC25 ; G6PC2	0.827	0.120	2	168906638	intron variant	T/C	snv	0.79	0.80	18
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
rs174550	FADS1 ; FADS2	0.925	0.160	11	61804006	5 prime UTR variant	T/C	snv		0.28	13
rs2068834	ZNF512	0.925	0.120	2	27616672	intron variant	T/C	snv		0.28	10
rs2657879	GLS2 ; SPRYD4	1.000	0.080	12	56471554	missense variant	A/G	snv	0.17	0.15	9
rs1799884	GCK	1.000	0.080	7	44189469	intron variant	C/T	snv		0.17	6
rs2851682	FADS2			11	61848540	intron variant	A/G	snv		9.9E-02	5
rs853789	ABCB11			2	168944978	intron variant	A/G;T	snv	0.75		4