DisGeNET - a database of gene-disease associations

List of shared variants

Hypodontia, C0020608

Disease: Developmental absence of tooth

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
rs121908120	WNT10A	0.701	0.280	2	218890289	missense variant	T/A	snv	1.4E-02	1.4E-02	19
rs121908119	WNT10A ; LOC107984111	0.763	0.200	2	218882368	stop gained	C/A	snv	6.2E-04	8.5E-04	10
rs2034604	ARHGAP15	0.776	0.160	2	143201176	intron variant	C/G;T	snv			8
rs35822372		0.776	0.160	2	88438931	intergenic variant	C/A;T	snv			8
rs35956082	FOXP1	0.776	0.160	3	71414748	intron variant	A/C;G	snv			8
rs4498834	CACNA1S	0.776	0.160	1	201111170	intron variant	T/C	snv		0.56	8
rs55846652		0.776	0.160	X	69564858	downstream gene variant	T/C	snv		0.29	8
rs758468472	NOL11 ; LOC101928045	0.776	0.160	17	67718094	splice region variant	G/T	snv			8
rs917412		0.776	0.160	4	108350621	TF binding site variant	C/T	snv		0.21	8
rs4904210	PAX9	0.851	0.080	14	36666548	missense variant	G/C	snv	0.36	0.33	5