Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057519925
rs1057519925
PIK3CA
A 0.700 CausalMutation CLINVAR

dbSNP: rs1131692227
rs1131692227
KDM5C
T 0.700 CausalMutation CLINVAR

dbSNP: rs114925667
rs114925667
UBA5 ; NPHP3-ACAD11
A 0.700 CausalMutation CLINVAR

dbSNP: rs1276519904
rs1276519904
H3-3A
G 0.700 GeneticVariation CLINVAR

dbSNP: rs138632121
rs138632121
HCFC1R1 ; THOC6
A 0.700 CausalMutation CLINVAR

dbSNP: rs1568507354
rs1568507354
RYR1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs200426926
rs200426926
THOC6 ; BICDL2
A 0.700 CausalMutation CLINVAR

dbSNP: rs200661329
rs200661329
PIGQ
A 0.700 GeneticVariation CLINVAR

dbSNP: rs374052333
rs374052333
UBA5 ; NPHP3-ACAD11
T 0.700 GeneticVariation CLINVAR

dbSNP: rs75184679
rs75184679
RNASEH2B
A 0.700 CausalMutation CLINVAR

dbSNP: rs81002885
rs81002885
BRCA2
C 0.700 CausalMutation CLINVAR

dbSNP: rs4647924
rs4647924
FGFR3
0.010 GeneticVariation BEFREE To determine whether the autosomal dominant fibroblast growth factor receptor 3 (FGFR3) Pro250Arg mutation causes anterior plagiocephaly, patients with either apparently sporadic unicoronal synostosis (N = 37) or other forms of anterior plagiocephaly (N = 10) were studied for this mutation. 9580776

1998