DisGeNET - a database of gene-disease associations

Disease: Birth Weight

Source: ALL

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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 GENOME	Num. diseases
rs7903146	TCF7L2	0.554	0.680	10	112998590	intron variant	C/G;T	snv		93
rs798489	GNA12 ; AMZ1			7	2762169	splice donor variant	C/T	snv	0.20	4
rs1482852	LINC02029			3	157080505	upstream gene variant	A/G	snv	0.46	2