DisGeNET - a database of gene-disease associations

List of shared variants

Follicular thyroid carcinoma, C0206682

Disease: Malignant neoplasm of thyroid

Source: ALL

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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
rs113488022	BRAF	0.351	0.840	7	140753336	missense variant	A/C;G;T	snv	4.0E-06		490
rs121913377	BRAF	0.354	0.840	7	140753335	missense variant	CA/AT;TT	mnv			480
rs11554290	NRAS	0.583	0.600	1	114713908	missense variant	T/A;C;G	snv			59
rs1057519695	NRAS	0.641	0.520	1	114713907	missense variant	TT/CA;CC	mnv			35
rs1057519834	NRAS	0.658	0.480	1	114713908	missense variant	TG/CT	mnv			31
rs1799939	RET	0.658	0.280	10	43114671	missense variant	G/A;C;T	snv	0.21		27
rs944289		0.742	0.200	14	36180040	upstream gene variant	C/T	snv		0.45	16
rs11214077	SDHD ; TIMM8B	0.752	0.120	11	112087953	missense variant	A/G	snv	6.6E-03	6.7E-03	12
rs17849071	PIK3CA	0.776	0.160	3	179218439	intron variant	T/G	snv		7.9E-02	8