DisGeNET - a database of gene-disease associations

List of shared variants

Triglycerides measurement, C0202236

Disease: Red Blood Cell Count measurement

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
rs780094	GCKR	0.658	0.400	2	27518370	intron variant	T/C	snv		0.67	62
rs7412	APOE	0.641	0.640	19	44908822	missense variant	C/T	snv	6.2E-02	7.9E-02	47
rs495828		0.827	0.200	9	133279294	upstream gene variant	T/G	snv		0.81	24
rs102275	TMEM258	0.827	0.320	11	61790331	non coding transcript exon variant	T/C	snv		0.47	18
rs2070895	LIPC ; ALDH1A2	0.807	0.120	15	58431740	intron variant	G/A	snv		0.33	15
rs28601761		1.000	0.040	8	125487789	intron variant	C/G	snv		0.37	13
rs13389219	COBLL1	1.000	0.080	2	164672366	intron variant	C/T	snv		0.47	9
rs605066				6	139508529	intron variant	C/T	snv		0.53	6
rs634869				6	139510620	intron variant	T/A;C	snv			5
rs150844304	TP53BP1			15	43434427	intron variant	A/C;G	snv			4
rs1936807	RSPO3			6	127127104	intron variant	C/G	snv		0.55	4