DisGeNET - a database of gene-disease associations

Source: GWASCAT

Variants associated to the Gene: PTPRN2 ×

Results per page

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
rs11765189	PTPRN2	1.000	0.040	7	157743285	intron variant	A/G	snv		0.25	3
rs2533291	PTPRN2	0.925	0.120	7	157712962	intron variant	C/T	snv		0.12	2
rs4272321	PTPRN2	1.000	0.080	7	158159143	intron variant	A/G	snv		4.6E-04	2
rs10949662	PTPRN2			7	157741413	intron variant	C/A;T	snv			2
rs1242780	PTPRN2	1.000	0.080	7	157757146	intron variant	T/G	snv		0.25	2
rs117114682	PTPRN2	0.925	0.080	7	158170200	intron variant	A/G	snv		2.6E-02	2
rs7802459	PTPRN2	0.925	0.040	7	157712968	intron variant	T/C	snv		0.74	2
rs896773	PTPRN2	0.925	0.040	7	158359285	intron variant	C/G;T	snv			2
rs10274279	PTPRN2	1.000	0.040	7	157594749	intron variant	T/C	snv		0.17	1
rs10281741	PTPRN2			7	158000430	intron variant	G/A;C;T	snv			1
rs111630016	PTPRN2			7	158255704	intron variant	C/T	snv		3.8E-02	1
rs55770502	PTPRN2			7	157723280	intron variant	G/A;C	snv			1
rs56211164	PTPRN2			7	158224072	intron variant	G/A	snv		0.25	1
rs56283944	PTPRN2			7	158191148	intron variant	G/A;C	snv			1