DisGeNET - a database of gene-disease associations

Source: GWASCAT

Variants associated to the Disease: Mean Corpuscular Volume (result) ×

Variants associated to the Gene: CCND3 ×

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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
rs9349205	CCND3			6	41957421	intron variant	G/A;C	snv			6
rs112233623	CCND3			6	41957260	intron variant	C/T	snv		7.0E-03	5
rs3218097	CCND3			6	41937537	intron variant	G/A;T	snv			5
rs10947997	CCND3			6	41953503	intron variant	G/T	snv		0.13	2
rs11970772	CCND3			6	41957552	intron variant	T/A	snv		0.24	2
rs16895130	CCND3			6	41957193	intron variant	A/G	snv		0.22	2
rs9296369	CCND3			6	41953258	intron variant	C/G;T	snv			2
rs9349204	CCND3			6	41946640	intron variant	A/G;T	snv			1
rs4714548	CCND3 ; LOC105375059			6	42015693	intron variant	A/C;G;T	snv			1