DisGeNET - a database of gene-disease associations

List of associated variants

Iron binding capacity total measurement, C1283048

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
rs74138220	LOC105371657			1	189188129	intergenic variant	G/A	snv		3.8E-03	2
rs145285408	LOC105375153			7	11345523	intron variant	G/C	snv		2.4E-03	2
rs142692454	LOC105378648 ; LOC107984941			1	36686538	intergenic variant	A/G	snv		4.1E-03	2
rs16839481	NPHP3-ACAD11 ; ACAD11 ; UBA5			3	132660153	5 prime UTR variant	G/A	snv		1.1E-02	2
rs61740410	PRSS16			6	27256809	downstream gene variant	G/A	snv		4.2E-02	2
rs7637997	RAB6B			3	133864120	intron variant	G/A;C;T	snv			2
rs9824310	SCHIP1 ; IQCJ-SCHIP1			3	159474954	intron variant	A/G	snv		0.68	2
rs9872999	TF ; INHCAP			3	133738670	intron variant	C/G;T	snv			2
rs183511413	TMEM108			3	133330418	intron variant	A/G	snv		2.3E-04	2
rs192622883	TMEM108			3	133150563	intron variant	A/G	snv		2.5E-04	2