DisGeNET - a database of gene-disease associations

List of shared variants

Red cell distribution width determination, C0427460

Disease: Body Height

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
rs1260326	GCKR	0.645	0.600	2	27508073	missense variant	T/C;G	snv	0.63; 4.0E-06	0.68	81
rs11556924	ZC3HC1	0.752	0.240	7	130023656	missense variant	C/A;T	snv	4.0E-06; 0.28		21
rs2277339	HSD17B6 ; PRIM1			12	56752285	missense variant	T/G	snv	0.12	0.14	10
rs34651	TNPO1	1.000	0.040	5	72848178	non coding transcript exon variant	C/T	snv		0.94	5
rs1885486	LOC105374906			6	7695740	intergenic variant	G/A	snv		0.40	4
rs28673728	INPP5B ; LOC105378651			1	37943401	intron variant	A/G	snv		0.40	3
rs3218036	CCNE1			19	29814777	intron variant	G/A	snv		0.23	3
rs66969865	TMEM171			5	73124957	intron variant	C/T	snv		9.8E-02	3
rs9314323	BNIP3L			8	26385620	intron variant	A/G;T	snv			3
rs9623	PIK3R1			5	68301493	3 prime UTR variant	T/A;C	snv			3