DisGeNET - a database of gene-disease associations

Source: ALL

Variants associated to the Disease: Red cell distribution width determination ×

Variants associated to the Gene: SLC25A37 ×

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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
rs2942194	SLC25A37			8	23566156	missense variant	A/G	snv	0.25	0.21	3
rs10503728	SLC25A37			8	23563489	intron variant	A/C;G	snv			2