DisGeNET - a database of gene-disease associations

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Gene

Disease

Variant

Source

DSI _v

DPI _v

pLI

Consequence

AF_EXOME

AF_GENOME

Variant	Gene	Chr	Position	Consequence	Alleles	Class	AF EXOME	AF GENOME	Num. diseases
rs10224902	ANLN	7	36415868	synonymous variant	T/C	snv	0.13	0.12	2
rs3735398	ANLN	7	36406512	synonymous variant	A/G	snv	0.13	0.11	1
rs55891665	ANLN	7	36406903	intron variant	A/G	snv		0.12	1