DisGeNET - a database of gene-disease associations

Source: ALL

Variants associated to the Gene: GMDS ×

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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
rs115986297	GMDS			6	2050557	intron variant	A/C;G	snv			3
rs17134767	GMDS			6	2195682	intron variant	T/C	snv		0.31	2
rs722585	GMDS			6	1775629	intron variant	G/A	snv		0.25	2
rs11969985	GMDS	1.000	0.040	6	1922673	intron variant	G/A	snv		0.18	1
rs3778519	GMDS			6	1771278	intron variant	C/T	snv		0.26	1
rs3778523	GMDS			6	1777530	intron variant	T/C	snv		0.45	1
rs62390617	GMDS			6	1623392	downstream gene variant	G/A;C	snv			1
rs6914086	GMDS			6	2095801	intron variant	T/C	snv		0.58	1
rs7757144	GMDS			6	1997631	intron variant	A/G;T	snv			1
rs9378319	GMDS			6	2053443	intron variant	T/C	snv		0.19	1
rs9378671	GMDS			6	2040937	intron variant	T/C	snv		0.21	1
rs9392348	GMDS	1.000	0.040	6	1989370	intron variant	G/A	snv		0.20	1
rs9405157	GMDS			6	1988690	intron variant	T/C	snv		0.24	1
rs9503012	LOC107986513 ; GMDS	1.000	0.040	6	1707020	intron variant	C/T	snv		0.63	1