DisGeNET - a database of gene-disease associations

List of associated variants

Phosphorus measurement, C0202178

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 EXOME	AF GENOME	Num. diseases
rs17265703	CSTA			3	122329797	intron variant	A/G	snv		0.12	4
rs4074995	RGS14			5	177370342	intron variant	G/A	snv		0.23	4
rs1106357				1	21490592	intergenic variant	C/T	snv		0.37	3
rs1697421				1	21496799	intergenic variant	C/A;T	snv			3
rs35716097	SLC34A1			5	177379635	intron variant	C/T	snv		0.34	3
rs12368351				12	4426615	downstream gene variant	G/A	snv		0.24	2
rs17060705				6	131765353	TF binding site variant	G/A	snv		8.8E-02	2
rs3903005				12	12010749	intergenic variant	C/G	snv		0.89	2
rs2275372	ALPL			1	21573903	intron variant	A/C	snv		0.19	2
rs2970818	C12orf4			12	4497002	intron variant	T/A;C	snv			2
rs453639	ENPP3			6	131728517	intron variant	C/A	snv		0.75	2
rs73743323	IP6K3			6	33737578	intron variant	C/T	snv		0.11	2
rs9469578	IP6K3			6	33738702	intron variant	C/T	snv		0.11	2
rs947583	LINC00271			6	135812521	non coding transcript exon variant	T/C	snv		0.27	2
rs35186465	LINC01482			17	68685441	intron variant	G/A	snv		0.19	2
rs178710	PHEX			X	22032916	5 prime UTR variant	A/G	snv			2
rs2275360	RAP1GAP			1	21617327	synonymous variant	G/A	snv	0.32	0.26	2