Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs797044834
rs797044834
DVL1
G 0.700 CausalMutation CLINVAR WNT Signaling Perturbations Underlie the Genetic Heterogeneity of Robinow Syndrome. 29276006

2018
dbSNP: rs869025220
rs869025220
DVL1
A 0.700 CausalMutation CLINVAR DVL3 Alleles Resulting in a -1 Frameshift of the Last Exon Mediate Autosomal-Dominant Robinow Syndrome. 26924530

2016
dbSNP: rs797044833
rs797044833
DVL1
G 0.700 CausalMutation CLINVAR DVL1 frameshift mutations clustering in the penultimate exon cause autosomal-dominant Robinow syndrome. 25817016

2015
dbSNP: rs797044834
rs797044834
DVL1
G 0.700 CausalMutation CLINVAR DVL1 frameshift mutations clustering in the penultimate exon cause autosomal-dominant Robinow syndrome. 25817016

2015
dbSNP: rs797044835
rs797044835
DVL1
C 0.700 CausalMutation CLINVAR DVL1 frameshift mutations clustering in the penultimate exon cause autosomal-dominant Robinow syndrome. 25817016

2015
dbSNP: rs797044836
rs797044836
DVL1
C 0.700 CausalMutation CLINVAR DVL1 frameshift mutations clustering in the penultimate exon cause autosomal-dominant Robinow syndrome. 25817016

2015
dbSNP: rs797044837
rs797044837
DVL1
C 0.700 CausalMutation CLINVAR DVL1 frameshift mutations clustering in the penultimate exon cause autosomal-dominant Robinow syndrome. 25817016

2015
dbSNP: rs797044838
rs797044838
DVL1
A 0.700 CausalMutation CLINVAR DVL1 frameshift mutations clustering in the penultimate exon cause autosomal-dominant Robinow syndrome. 25817016

2015
dbSNP: rs1223920489
rs1223920489
FZD2
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1553173367
rs1553173367
DVL1
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1553173368
rs1553173368
DVL1
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1553173372
rs1553173372
DVL1
GCTGCC 0.700 GeneticVariation CLINVAR

dbSNP: rs1553173420
rs1553173420
DVL1
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1553811652
rs1553811652
DVL3
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1555657045
rs1555657045
FZD2
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1555657074
rs1555657074
FZD2
TT 0.700 GeneticVariation CLINVAR

dbSNP: rs1568105666
rs1568105666
FZD2
A 0.700 CausalMutation CLINVAR

dbSNP: rs797044839
rs797044839
DVL1
T 0.700 CausalMutation CLINVAR

dbSNP: rs797044840
rs797044840
DVL1
C 0.700 CausalMutation CLINVAR