DisGeNET - a database of gene-disease associations

List of shared variants

Malignant Uterine Corpus Neoplasm, C0153574

Disease: Multiple Myeloma

Source: CLINVAR ×

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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	Num. diseases
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
rs1057519933	PIK3CA	0.790	0.240	3	179199156	missense variant	A/G	snv		11
rs1057519935	PIK3CA	0.790	0.240	3	179199157	missense variant	A/G	snv		11
rs1057519934	PIK3CA	0.790	0.240	3	179199158	missense variant	G/C	snv		11
rs17851045	KRAS	0.672	0.400	12	25227341	missense variant	T/A;G	snv	4.0E-06	15
rs121913233	HRAS ; LRRC56	0.627	0.520	11	533874	missense variant	T/A;C;G	snv		20
rs28933406	LRRC56 ; HRAS	0.667	0.480	11	533875	missense variant	G/C;T	snv		17
rs104894226	LRRC56 ; HRAS	0.658	0.560	11	534285	missense variant	C/A;G;T	snv		23
rs104894228	LRRC56 ; HRAS	0.605	0.560	11	534286	missense variant	C/A;G;T	snv		30
rs104894230	HRAS ; LRRC56	0.564	0.600	11	534288	missense variant	C/A;G;T	snv		36
rs104894229	LRRC56 ; HRAS	0.564	0.600	11	534289	missense variant	C/A;G;T	snv		52
rs587781525	TP53	0.689	0.480	17	7673778	missense variant	T/A;C;G	snv		20
rs764146326	TP53	0.662	0.480	17	7673779	missense variant	C/A;G;T	snv	4.0E-06	20
rs876659802	TP53	0.732	0.440	17	7673787	missense variant	G/A;C;T	snv		15
rs17849781	TP53	0.701	0.480	17	7673788	missense variant	G/A;C;T	snv		14
rs28934576	TP53	0.554	0.600	17	7673802	missense variant	C/A;G;T	snv	4.0E-06; 1.6E-05	39
rs121913343	TP53	0.611	0.520	17	7673803	missense variant	G/A;C;T	snv	1.2E-05	29
rs876660333	TP53	0.742	0.360	17	7673805	missense variant	A/C;G;T	snv		13
rs121912657	TP53	0.683	0.480	17	7673806	missense variant	C/A;G;T	snv	4.0E-06	15
rs11540652	TP53	0.592	0.640	17	7674220	missense variant	C/A;G;T	snv	1.2E-05	42
rs121912651	TP53	0.605	0.680	17	7674221	missense variant	G/A;C	snv	4.0E-06	37
rs730882005	TP53	0.701	0.400	17	7674250	missense variant	C/A;G;T	snv	8.0E-06	20