DisGeNET - a database of gene-disease associations

Source: GWASCAT

Variants associated to the Disease: Finding of Mean Corpuscular Hemoglobin ×

Variants associated to the Gene: NPRL3 ×

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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
rs7203560	NPRL3	1.000	0.080	16	134391	intron variant	T/G	snv		2.0E-02	6
rs117747069	NPRL3			16	120077	intron variant	G/C	snv		2.5E-02	4
rs2238368	NPRL3			16	120329	intron variant	C/T	snv		0.36	3
rs6600233	NPRL3			16	93505	intron variant	C/G;T	snv			2
rs11248850	NPRL3			16	113599	intron variant	G/A	snv		0.38	1
rs545105162	NPRL3			16	98445	intron variant	G/A	snv		5.4E-04	1
rs8055187	NPRL3			16	108326	intron variant	A/T	snv		0.37	1