DisGeNET - a database of gene-disease associations

Source: ALL

Variants associated to the Disease: Hepatitis B ×

Variants associated to the Gene: SLC10A1 ×

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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
rs2296651	SLC10A1	0.732	0.240	14	69778476	missense variant	G/A	snv	6.3E-03	2.5E-03	13
rs201339654	SLC10A1	0.925	0.080	14	69786192	missense variant	C/G;T	snv	8.0E-06; 2.0E-05		2
rs4646287	SLC10A1	0.925	0.120	14	69796098	intron variant	C/T	snv		3.3E-03	2
rs7154439	SLC10A1	0.925	0.120	14	69799111	upstream gene variant	G/A	snv		0.36	2
rs4646285	SLC10A1	1.000	0.080	14	69796931	synonymous variant	C/T	snv	9.7E-02	7.2E-02	1
rs943277	SLC10A1	1.000	0.080	14	69794608	intron variant	G/A	snv		0.13	1