DisGeNET - a database of gene-disease associations

Source: ALL

Variants associated to the Gene: SLC45A4 ×

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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
rs11167044	SLC45A4			8	141294322	intron variant	C/T	snv		0.84	1
rs12543725	SLC45A4			8	141237880	intron variant	G/A	snv		0.33	1
rs13257363	SLC45A4			8	141242481	intron variant	G/A	snv		0.33	1
rs59918340	SLC45A4			8	141222157	intron variant	A/G	snv		0.51	1
rs6987335	SLC45A4			8	141225259	non coding transcript exon variant	T/G	snv		0.33	1
rs6992286	SLC45A4			8	141269313	intron variant	G/A	snv		0.41	1
rs7014099	SLC45A4			8	141295667	intron variant	C/T	snv		0.30	1
rs753778	SLC45A4			8	141218810	missense variant	G/A	snv	0.35	0.33	1
rs919873	SLC45A4			8	141292161	intron variant	C/G;T	snv			1