DisGeNET - a database of gene-disease associations

List of shared variants

Blood Protein Measurement, C2985280

Disease: Finding of Mean Corpuscular Hemoglobin

Source: GWASCAT ×

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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
rs7412	APOE	0.641	0.640	19	44908822	missense variant	C/T	snv	6.2E-02	7.9E-02	20
rs855791	TMPRSS6	0.701	0.400	22	37066896	missense variant	A/G;T	snv	0.57; 4.0E-06		17
rs77542162	ABCA6	1.000	0.040	17	69085137	missense variant	A/G	snv	9.3E-03	1.0E-02	10
rs8176743	ABO	1.000	0.040	9	133256028	missense variant	C/T	snv	0.12	0.11	5
rs1958078	SMOC1			14	69888141	intron variant	A/C;G	snv			4
rs149037075	ABO			9	133255469	3 prime UTR variant	CTGT/-	delins		0.15	3
rs4499344	PDCD5			19	32582525	intron variant	G/A	snv		0.46	3
rs4729597	TFR2			7	100624226	intron variant	C/T	snv		0.69	2
rs72660908	RSRP1			1	25257119	intron variant	C/G	snv		0.26	2