DisGeNET - a database of gene-disease associations

List of associated variants

Robinow syndrome, autosomal recessive, C1849334

Source: UNIPROT ×

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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
rs121909084	ROR2	1.000	0.120	9	91737463	missense variant	G/A	snv	4.0E-06		1
rs199975149	ROR2	1.000	0.120	9	91737448	missense variant	G/A	snv	8.0E-06	2.1E-05	1