DisGeNET - a database of gene-disease associations

List of shared variants

Transferrin saturation measurement, C1277709

Disease: Serum iron measurement

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
rs1800562	LOC108783645 ; HFE	0.435	0.880	6	26092913	missense variant	G/A	snv	3.3E-02	3.8E-02	262
rs1799945	LOC108783645 ; HFE	0.452	0.760	6	26090951	missense variant	C/G;T	snv	0.11	0.10	226
rs855791	TMPRSS6	0.701	0.400	22	37066896	missense variant	A/G;T	snv	0.57; 4.0E-06		38
rs7385804	TFR2	0.851	0.120	7	100638347	intron variant	C/A	snv		0.65	14
rs8177240	TF			3	133758857	intron variant	T/C;G	snv		0.29	5
rs111722075	CMAHP ; CARMIL1			6	25373818	intron variant	C/T	snv		0.11	2
rs113507773	LOC105374986			6	26255511	upstream gene variant	G/A	snv		0.10	2
rs143130997	FIG4			6	109780207	intron variant	G/A	snv		5.9E-03	2
rs150548770	ESM1 ; LOC102467081			5	55020802	intron variant	T/C	snv		5.4E-03	2
rs181143083	ZDHHC14			6	157434218	intron variant	T/A	snv		7.5E-04	2
rs202056061	CARMIL1			6	25494109	intron variant	AGTT/-	delins		2.8E-02	2
rs2442120	DTWD2			5	118970884	intron variant	A/C	snv		0.98	2
rs73373322	SEPTIN9			17	77385957	intron variant	C/T	snv		3.1E-02	2