DisGeNET - a database of gene-disease associations

Variant: rs140948517 ×

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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
rs140948517	RHBDD2			7	75857462	intron variant	TT/-;T;TTT;TTTT;TTTTTTTTTTTT	delins			2