DisGeNET - a database of gene-disease associations

Results per page

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
rs7578597	THADA	0.807	0.240	2	43505684	missense variant	T/C	snv	9.9E-02	0.14	2
rs10495903	THADA	1.000	0.040	2	43579779	intron variant	C/T	snv		0.13	2
rs1465618	THADA	0.882	0.160	2	43326810	intron variant	T/C	snv		0.80	2
rs6729902	THADA	1.000	0.080	2	43349829	intron variant	C/T	snv		0.20	1
rs13035011	THADA	1.000	0.080	2	43316978	intron variant	C/T	snv		0.20	1
rs7590268	THADA	1.000	0.080	2	43312986	intron variant	T/G	snv		0.22	1
rs11899863	THADA	1.000	0.080	2	43391680	intron variant	C/T	snv		8.5E-02	1
rs10203174	THADA	1.000	0.080	2	43462891	intron variant	C/T	snv		0.17	1
rs17030845	THADA			2	43460740	intron variant	C/T	snv		0.11	1
rs12468394	THADA	1.000	0.120	2	43334022	intron variant	C/A	snv		0.48	1
rs6731009	THADA	1.000	0.120	2	43576289	intron variant	T/C	snv		0.34	1
rs6726014	THADA	1.000	0.120	2	43556155	3 prime UTR variant	A/T	snv		0.36	1
rs7582497	THADA	1.000	0.120	2	43411808	intron variant	T/C;G	snv			1
rs17030684	THADA	1.000	0.120	2	43320989	intron variant	G/A	snv		0.19	1
rs11891936	THADA	1.000	0.120	2	43305163	intron variant	C/T	snv		0.18	1
rs4340576	THADA	1.000	0.120	2	43328367	intron variant	T/C	snv		0.80	1
rs7559891	THADA	1.000	0.120	2	43539900	intron variant	G/A	snv		0.60	1
rs7567607	THADA	1.000	0.120	2	43411046	intron variant	C/T	snv		0.69	1
rs13429458	THADA	0.827	0.200	2	43411699	intron variant	A/C	snv		0.14	1
rs10179648	THADA	1.000	0.120	2	43580926	intron variant	C/T	snv		0.70	1
rs12478601	THADA	0.851	0.200	2	43494369	intron variant	C/T	snv		0.61	1
rs7568365	THADA	1.000	0.120	2	43411716	intron variant	C/T	snv		0.69	1
rs1873555	THADA	1.000	0.120	2	43552526	intron variant	T/C	snv		0.34	1
rs1038822	THADA	1.000	0.120	2	43511034	intron variant	T/A;C	snv			1