DisGeNET - a database of gene-disease associations

Source: GWASDB

Variants associated to the Disease: Protein C antigen measurement ×

Variants associated to the Gene: NFS1 ×

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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
rs11907022	NFS1			20	35695704	intron variant	A/G	snv		0.10	2
rs17336615	NFS1			20	35674089	non coding transcript exon variant	A/C;G	snv			2
rs2180280	NFS1			20	35669429	3 prime UTR variant	T/C	snv		6.7E-02	2
rs6060546	NFS1			20	35669741	intron variant	A/C;G	snv			2
rs6060548	NFS1			20	35676643	intron variant	T/A	snv		6.7E-02	2
rs6121023	NFS1			20	35668718	3 prime UTR variant	A/C	snv		6.7E-02	2
rs6121029	NFS1			20	35686515	intron variant	T/C	snv		0.10	2
rs3088078	NFS1 ; ROMO1 ; RBM39			20	35700932	3 prime UTR variant	C/T	snv	6.0E-02	3.7E-02	2