DisGeNET - a database of gene-disease associations

List of associated variants

Multiple Myeloma, C0026764

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 GENOME	Num. diseases
rs4525246	GRAMD1B	0.851	0.160	11	123524538	intron variant	G/A;C	snv		4
rs6535455	HPSE	0.851	0.160	4	83310951	intron variant	T/A;C	snv		4
rs6546149	DTNB	0.851	0.160	2	25406569	intron variant	C/G	snv	0.38	4
rs6763508	ULK4	0.851	0.160	3	41709497	intron variant	T/C	snv	0.30	4
rs73005220	CIB3	0.851	0.160	19	16161878	intron variant	A/G	snv	3.9E-02	4
rs7372217	ULK4	1.000	0.160	3	41948630	intron variant	G/A	snv	0.68	4
rs7651190	ULK4	1.000	0.160	3	41724463	intron variant	A/G	snv	0.33	4
rs974120		0.851	0.200	8	2789080	intron variant	T/C;G	snv		4
rs9815354	ULK4	0.925	0.160	3	41871159	intron variant	G/A;T	snv		4
rs138740	TOM1	0.882	0.160	22	35303589	intron variant	C/T	snv	0.51	3
rs1716983	ULK4	1.000	0.160	3	41922636	intron variant	G/A;C;T	snv		3
rs1717027	ULK4	1.000	0.160	3	41946428	intron variant	T/A;C	snv		3
rs4487645	DNAH11	0.882	0.200	7	21898622	intron variant	C/A;T	snv		3
rs56219066	ELL2	0.882	0.160	5	95907227	intron variant	T/A;C	snv		3
rs57104699	DNAH11	0.882	0.160	7	21888461	intron variant	C/A	snv	0.26	3
rs73071352	ULK4	0.882	0.160	3	41786808	intron variant	A/G	snv	0.12	3
rs73081364	ULK4	1.000	0.160	3	41872124	intron variant	G/A;C;T	snv		3
rs7622665	ULK4	1.000	0.160	3	41929251	intron variant	T/C	snv	0.67	3
rs879882	POU5F1	1.000	0.160	6	31171675	intron variant	T/C;G	snv		3
rs9848754	ULK4	0.882	0.160	3	41712155	intron variant	C/T	snv	0.18	3
rs10936601	LRRC34	1.000	0.160	3	169810661	intron variant	C/T	snv	0.37	2
rs2285803	PSORS1C2 ; PSORS1C1	0.925	0.160	6	31139481	intron variant	T/C	snv	0.72	2
rs2683696	ULK4	1.000	0.160	3	41873406	intron variant	T/C	snv	0.34	2
rs28581706	ULK4	1.000	0.160	3	41829905	intron variant	A/C;T	snv		2
rs2903754	ANKRD27	0.925	0.200	19	32600776	intron variant	C/T	snv	0.62	2