DisGeNET - a database of gene-disease associations

List of associated variants

Malignant Uterine Corpus Neoplasm, C0153574

Source: CLINVAR ×

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
rs1057519915	MTOR	0.851	0.160	1	11109318	missense variant	A/C	snv			5
rs1057519916	MTOR	0.882	0.160	1	11109320	missense variant	T/A	snv			4
rs587777894	MTOR	0.776	0.240	1	11124516	missense variant	G/A;T	snv			9
rs1057519917	MTOR	0.807	0.160	1	11124517	missense variant	A/G;T	snv			7
rs121913255	NRAS	0.667	0.400	1	114713907	missense variant	T/A;G	snv			19
rs11554290	NRAS	0.583	0.600	1	114713908	missense variant	T/A;C;G	snv			25
rs121913237	NRAS	0.611	0.560	1	114716126	missense variant	C/A;G;T	snv	8.0E-06		12
rs121913250	NRAS	0.683	0.440	1	114716127	missense variant	C/A;G;T	snv			12
rs1057519854	FGFR2	0.882	0.080	10	121488063	missense variant	A/T	snv			5
rs121913476	FGFR2	0.851	0.080	10	121498520	missense variant	A/C;T	snv			5
rs1057519045	FGFR2	0.851	0.160	10	121498522	missense variant	T/G	snv			6
rs1057519901	FGFR2	0.925	0.080	10	121498525	missense variant	T/G	snv			5
rs1057519900	FGFR2	0.882	0.120	10	121515259	missense variant	C/T	snv			3
rs121913474	FGFR2	0.790	0.200	10	121515260	missense variant	A/G	snv			3
rs387906678	FGFR2	0.851	0.120	10	121515263	missense variant	A/C;G	snv			5
rs79184941	FGFR2	0.617	0.600	10	121520163	missense variant	G/A;C	snv	5.6E-05; 4.0E-06		18
rs1057519945	POLE	0.776	0.200	12	132673703	missense variant	C/A;T	snv			4
rs1057519943	POLE	0.790	0.160	12	132676598	missense variant	G/C;T	snv			5
rs1057519944	POLE	0.882	0.160	12	132676599	missense variant	G/A	snv			5
rs121913365	BRAF	0.776	0.320	7	140753332	missense variant	T/A;G	snv			8
rs397507484	BRAF	0.752	0.480	7	140753333	missense variant	T/A;C;G	snv			10
rs121913364	BRAF	0.641	0.520	7	140753334	missense variant	T/C;G	snv	4.0E-06		14
rs1057519950	RHEB	0.827	0.200	7	151490963	missense variant	T/A;C	snv			4
rs1057519949	RHEB	0.851	0.120	7	151490964	missense variant	A/T	snv			4
rs759610249	FBXW7	0.790	0.160	4	152323032	missense variant	C/T	snv	8.0E-06	7.0E-06	8