DisGeNET - a database of gene-disease associations

List of associated variants

Fatty acid measurement, C1281901

Source: ALL

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Gene

Disease

Variant

Source

DSI _v

DPI _v

pLI

Consequence

AF_EXOME

AF_GENOME

Variant	Gene	Chr	Position	Consequence	Alleles	Class	AF GENOME	Num. diseases
rs10502435	GREB1L	18	21527130	downstream gene variant	C/T	snv	0.15	1
rs9315681	LHFPL6	13	39409534	intron variant	A/C	snv	0.28	1
rs9566421	LHFPL6	13	39406692	intron variant	A/G	snv	0.28	1
rs9566425	LHFPL6	13	39408007	intron variant	A/G	snv	0.28	1
rs9576788	LHFPL6	13	39406548	intron variant	G/A	snv	0.28	1
rs9576793	LHFPL6	13	39408995	intron variant	G/C;T	snv		1
rs6683451	LINC01036 ; ERVMER61-1	1	187323476	intron variant	A/C	snv	7.1E-02	1
rs10518201	LOC101928893	4	78730706	regulatory region variant	A/G	snv	6.2E-02	1
rs12648219	LOC101928893	4	78734132	regulatory region variant	A/G	snv	0.17	1
rs17003427	LOC101928893	4	78721263	intergenic variant	C/T	snv	9.3E-02	1
rs1978552	LOC101928893	4	78742859	intergenic variant	G/T	snv	0.17	1
rs6839280	LOC101928893	4	78736218	regulatory region variant	T/C	snv	0.17	1
rs6857679	LOC101928893	4	78736206	regulatory region variant	C/T	snv	0.17	1
rs727760	LOC101928893	4	78738610	regulatory region variant	A/G	snv	0.17	1
rs727761	LOC101928893	4	78738511	regulatory region variant	A/C	snv	0.17	1
rs7439893	LOC101928893	4	78738019	regulatory region variant	A/G	snv	9.6E-02	1
rs9992277	LOC101928893	4	78740464	regulatory region variant	G/A	snv	0.17	1
rs17079653	LOC105370115	13	23959467	intron variant	A/G;T	snv		1
rs34440628	LOC105373898 ; LOC105373899	2	221659167	intergenic variant	G/A;C	snv		1
rs11695051	LOC107985897 ; SFXN5	2	73007303	intron variant	T/C	snv	5.2E-02	1
rs6986921	LOC401478	8	137853313	intron variant	G/A	snv	0.18	1
rs17112580	LOC728755	14	27352193	intron variant	G/A;T	snv		1
rs12580543	LPCAT3 ; C1S ; EMG1	12	6992881	intron variant	A/C	snv	0.12	1
rs11133865	MYO10	5	16854596	intron variant	T/C	snv	0.30	1
rs13361131	MYO10	5	16804871	intron variant	A/G	snv	6.1E-02	1