DisGeNET - a database of gene-disease associations

Source: ALL

Variants associated to the Disease: POLYDACTYLY, PREAXIAL II (disorder) ×

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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
rs587779752	LMBR1	0.882	0.120	7	156791474	intron variant	G/A	snv		7.0E-06	3
rs606231149	LMBR1	0.925	0.120	7	156791547	intron variant	A/G	snv			2
rs606231150	LMBR1	0.925	0.120	7	156791137	intron variant	T/C	snv			2
rs606231151	LMBR1	0.925	0.120	7	156791255	intron variant	G/C	snv			2
rs606231152	LMBR1	0.925	0.120	7	156791581	intron variant	A/G;T	snv			2
rs606231146	LMBR1	1.000	0.120	7	156791771	intron variant	G/A;C	snv			1
rs606231148	LMBR1	1.000	0.120	7	156791571	intron variant	T/A	snv			1
rs606231153	LMBR1	1.000	0.120	7	156791480	intron variant	G/A	snv			1
rs606231230	LMBR1	1.000	0.120	7	156791579	intron variant	C/T	snv			1
rs606231231	LMBR1	1.000	0.120	7	156791542	intron variant	A/C	snv			1