Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894193
rs104894193
ALX4
0.800 GeneticVariation UNIPROT Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defects. 11137991

2001
dbSNP: rs104894196
rs104894196
ALX4
0.800 GeneticVariation UNIPROT Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defects. 11137991

2001
dbSNP: rs104894193
rs104894193
ALX4
0.800 GeneticVariation UNIPROT The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500). 11106354

2000
dbSNP: rs104894196
rs104894196
ALX4
0.800 GeneticVariation UNIPROT The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500). 11106354

2000
dbSNP: rs104894193
rs104894193
ALX4
T 0.800 CausalMutation CLINVAR

dbSNP: rs104894196
rs104894196
ALX4
G 0.800 CausalMutation CLINVAR

dbSNP: rs104894191
rs104894191
ALX4
A 0.700 CausalMutation CLINVAR

dbSNP: rs104894192
rs104894192
ALX4
A 0.700 CausalMutation CLINVAR

dbSNP: rs104894197
rs104894197
ALX4
T 0.700 CausalMutation CLINVAR

dbSNP: rs387906325
rs387906325
ALX4
G 0.700 CausalMutation CLINVAR

dbSNP: rs587776614
rs587776614
ALX4
C 0.700 CausalMutation CLINVAR

dbSNP: rs587777700
rs587777700
ALX4
C 0.700 CausalMutation CLINVAR

dbSNP: rs587777702
rs587777702
ALX4
AGTTGCCATCTCTGTTGAGATCTTAG 0.700 CausalMutation CLINVAR