DisGeNET - a database of gene-disease associations

List of shared variants

Serum gamma-glutamyl transferase measurement, C1278049

Disease: C-reactive protein measurement

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
rs1169288	HNF1A-AS1 ; HNF1A	0.776	0.160	12	120978847	missense variant	A/C;T	snv	0.35		21
rs2393791	HNF1A	0.925	0.160	12	120986153	intron variant	C/T	snv		0.62	8
rs7310409	HNF1A	0.925	0.160	12	120987058	intron variant	A/C;G;T	snv			7
rs1169313	C12orf43			12	121004867	intron variant	T/A;C	snv			6
rs3213545	OASL			12	121033534	synonymous variant	G/A	snv	0.32	0.26	3
rs340005	RORA-AS1 ; RORA			15	60585831	intron variant	G/A	snv		0.67	3
rs7979473	HNF1A			12	120982457	intron variant	A/C;G	snv			2
rs7979478	HNF1A			12	120982460	intron variant	A/C;G;T	snv			2