DisGeNET - a database of gene-disease associations

Source: ALL

Variants associated to the Gene: DNMT1 ×

Results per page

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
rs2228611	DNMT1	0.708	0.520	19	10156401	synonymous variant	T/A;C	snv	0.52		19
rs16999593	DNMT1	0.742	0.240	19	10180505	missense variant	T/C	snv	2.4E-02	9.6E-03	14
rs2228612	DNMT1	0.763	0.160	19	10162696	missense variant	T/A;C;G	snv	0.14		12
rs10409243	S1PR2 ; DNMT1			19	10222312	3 prime UTR variant	C/A;G;T	snv			6
rs2288349	DNMT1	0.882	0.120	19	10146569	intron variant	G/A	snv	0.36	0.35	5
rs759920	DNMT1	0.882	0.120	19	10174102	intron variant	A/G;T	snv			3
rs10420321	DNMT1	0.925	0.080	19	10189741	intron variant	A/G	snv		0.11	2
rs11085721	DNMT1	1.000	0.120	19	10207300	intron variant	G/C	snv		0.13	2
rs1419316960	DNMT1	0.925	0.080	19	10166651	missense variant	T/C	snv		7.0E-06	2
rs2162560	DNMT1	1.000	0.040	19	10168778	intron variant	G/A	snv		0.35	2
rs994411260	DNMT1	0.925	0.160	19	10194877	missense variant	G/C	snv			2
rs10418707	DNMT1	1.000	0.040	19	10145541	intron variant	G/A;T	snv		0.11	1
rs10423341	DNMT1	1.000	0.040	19	10156590	intron variant	C/A	snv		0.13	1
rs11085720	DNMT1			19	10207087	intron variant	A/G	snv		0.54	1
rs1359908894	DNMT1	1.000	0.040	19	10154757	missense variant	G/T	snv	4.0E-06		1
rs1568234664	DNMT1	1.000	0.080	19	10154774	splice acceptor variant	C/A	snv			1
rs16999358	DNMT1	1.000	0.080	19	10162679	synonymous variant	G/A	snv	6.2E-03	2.4E-03	1
rs199473690	DNMT1	1.000	0.080	19	10155017	missense variant	T/C	snv			1
rs199473691	DNMT1	1.000	0.080	19	10155029	missense variant	GGA/TAT	mnv			1
rs199473692	DNMT1	1.000	0.080	19	10155018	missense variant	A/G	snv			1
rs2114724	DNMT1	1.000	0.040	19	10154572	intron variant	T/C	snv	0.52	0.51	1
rs397509391	DNMT1	1.000		19	10154602	missense variant	C/A	snv			1
rs397509392	DNMT1	1.000		19	10154709	missense variant	G/A;C	snv			1
rs397509393	DNMT1	1.000		19	10154604	missense variant	C/G;T	snv			1
rs4804490	DNMT1			19	10156335	intron variant	C/A	snv		0.11	1