DisGeNET - a database of gene-disease associations

Source: GWASDB

Variants associated to the Gene: ESR2 ×

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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
rs11850375	ESR2			14	64244659	intron variant	C/T	snv		4.4E-02	2
rs10459452	ESR2			14	64245143	intron variant	A/G	snv		4.4E-03	1
rs4365213	ESR2	1.000	0.080	14	64253546	intron variant	T/C	snv		0.41	1
rs1256030	ESR2	0.827	0.240	14	64280452	intron variant	A/G;T	snv			1
rs1256031	ESR2	0.790	0.200	14	64279461	intron variant	G/A;T	snv		0.57	1
rs1256033	ESR2			14	64278681	intron variant	T/A;C	snv			1
rs1256061	ESR2			14	64236875	intron variant	G/A;T	snv			1
rs12435857	ESR2	0.925	0.200	14	64256807	intron variant	G/A	snv		0.41	1
rs1152591	ESR2 ; SYNE2	1.000	0.080	14	64214130	intron variant	A/C;G;T	snv			1