DisGeNET - a database of gene-disease associations

List of associated variants

Fasting blood sugar result, C1261430

Source: GWASDB ×

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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 GENOME	Num. diseases
rs2971671	LOC105375257 ; GCK			7	44171738	intron variant	T/C	snv	0.22	2
rs2979422	POLD2			7	44122756	intron variant	T/C	snv	0.20	2
rs6943153	GRB10			7	50723882	intron variant	T/C	snv	0.56	2
rs6975024	GCK			7	44192287	intron variant	T/C	snv	0.14	2
rs749067	MADD			11	47296606	intron variant	T/C	snv	0.26	2
rs4665965	MPV17	0.925	0.120	2	27313513	intron variant	T/A;C	snv		4
rs16980051	SYMPK			19	45842628	non coding transcript exon variant	T/A;C	snv	0.47	2
rs11920090	SLC2A2	1.000	0.040	3	170999732	intron variant	T/A	snv	0.20	3
rs17712208	PROX1-AS1			1	213977102	intron variant	T/A	snv	2.1E-02	2
rs174537	TMEM258 ; MYRF	0.708	0.400	11	61785208	non coding transcript exon variant	G/T	snv	0.28	5
rs2191349		1.000	0.080	7	15024684	intergenic variant	G/T	snv	0.54	4
rs4402960	IGF2BP2	0.724	0.400	3	185793899	intron variant	G/T	snv	0.38	4
rs1983127	HKDC1 ; LOC101928994			10	69230145	intron variant	G/T	snv	0.38	2
rs3783347	WARS1			14	100372924	intron variant	G/T	snv	0.16	2
rs340878	PROX1-AS1 ; PROX1			1	213983706	intron variant	G/C	snv	0.63	2
rs12255372	TCF7L2	0.667	0.480	10	113049143	intron variant	G/A;T	snv		3
rs10747083				12	132465032	downstream gene variant	G/A;T	snv		2
rs11891554	PPM1G			2	27390750	intron variant	G/A;T	snv	7.1E-02	2
rs6113722	LINC00261			20	22576461	intron variant	G/A;T	snv		2
rs4237150	GLIS3			9	4290085	intron variant	G/A;C;T	snv		2
rs13023194		0.925	0.120	2	27744393	intergenic variant	G/A;C	snv		4
rs4607517	GCK	0.882	0.080	7	44196069	intron variant	G/A;C	snv		3
rs10758593	GLIS3	0.827	0.240	9	4292083	intron variant	G/A	snv	0.45	4
rs11603334	ARAP1	1.000	0.080	11	72721940	5 prime UTR variant	G/A	snv	0.12	4
rs13404446	TRIM54	0.925	0.120	2	27296386	intron variant	G/A	snv	0.42	4