DisGeNET - a database of gene-disease associations

Source: GWASDB

Variants associated to the Disease: Serum total cholesterol measurement ×

Variants associated to the Gene: TXNL4B ×

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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
rs2000999	HPR ; TXNL4B	1.000	0.080	16	72074194	intron variant	G/A	snv		0.16	4
rs217181	TXNL4B			16	72080103	intron variant	C/T	snv		0.20	2
rs16973640	TXNL4B			16	72050235	intron variant	T/G	snv		4.4E-02	1
rs7191270	TXNL4B			16	72051096	intron variant	T/C	snv		4.4E-02	1