DisGeNET - a database of gene-disease associations

Source: ALL

Variants associated to the Gene: HTR1B ×

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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
rs6296	HTR1B ; LOC105377864	0.732	0.160	6	77462543	synonymous variant	C/G	snv	0.31	0.27	23
rs11568817	HTR1B ; LOC105377864	0.790	0.120	6	77463665	5 prime UTR variant	A/C	snv		0.37	8
rs130058	HTR1B ; LOC105377864	0.790	0.120	6	77463564	5 prime UTR variant	T/A;G	snv			8
rs13212041	LOC105377864 ; HTR1B	0.851	0.200	6	77461407	downstream gene variant	C/T	snv		0.70	6
rs6298	HTR1B ; LOC105377864	0.925	0.040	6	77463275	synonymous variant	G/A	snv	0.31	0.27	2
rs130060	LOC105377864 ; HTR1B			6	77463033	missense variant	A/C;G	snv	9.9E-03; 4.0E-06		1
rs201815520	LOC105377864 ; HTR1B	1.000	0.080	6	77463302	synonymous variant	G/A	snv		1.4E-05	1
rs6297	LOC105377864 ; HTR1B			6	77462224	3 prime UTR variant	C/A;T	snv	0.89		1
rs757059851	LOC105377864 ; HTR1B			6	77462625	missense variant	G/T	snv	4.0E-06		1