DisGeNET - a database of gene-disease associations

List of associated variants

Transferrin saturation measurement, C1277709

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
rs10097946	KCNU1 ; LOC105379375			8	36920273	intron variant	C/A	snv		1.0E-02	1
rs138584487	LARGE1			22	33416876	intron variant	G/A;C	snv			1
rs116112266	LINC01885			2	107482651	intron variant	G/C	snv		3.5E-03	1
rs184908836	LINC02008			3	82041833	intron variant	A/G	snv		3.8E-03	1
rs57620710	LOC105370504 ; LINC02331			14	53694373	intron variant	GGAGGT/-	delins		0.78	1
rs140911738	MAPRE1			20	32849813	3 prime UTR variant	G/C	snv		9.3E-03	1
rs3797579	POLK			5	75574232	intron variant	A/G	snv		9.9E-04	1
rs35237909	PRSS16			6	27256188	3 prime UTR variant	ATCT/-	delins		4.2E-02	1
rs144453006	SLC3A2			11	62887212	intron variant	G/A	snv		3.2E-03	1
rs73214671	SORCS2			4	7570384	intron variant	G/A	snv		1.5E-02	1
rs17052130	SPRY3			X	155675419	intergenic variant	T/C	snv		4.0E-02	1