DVL3, dishevelled segment polarity protein 3, 1857

N. diseases: 167; N. variants: 6
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs869025215
rs869025215
Entrez Id: 1857
Gene Symbol: DVL3
DVL3
CUI: C4551475
Disease:
ROBINOW SYNDROME, AUTOSOMAL DOMINANT 1
C 0.700 CausalMutation CLINVAR DVL3 Alleles Resulting in a -1 Frameshift of the Last Exon Mediate Autosomal-Dominant Robinow Syndrome. 26924530 2016
dbSNP: rs869025216
rs869025216
Entrez Id: 1857
Gene Symbol: DVL3
DVL3
CUI: C4551475
Disease:
ROBINOW SYNDROME, AUTOSOMAL DOMINANT 1
G 0.700 CausalMutation CLINVAR DVL3 Alleles Resulting in a -1 Frameshift of the Last Exon Mediate Autosomal-Dominant Robinow Syndrome. 26924530 2016
dbSNP: rs869025217
rs869025217
Entrez Id: 1857
Gene Symbol: DVL3
DVL3
CUI: C4551475
Disease:
ROBINOW SYNDROME, AUTOSOMAL DOMINANT 1
A 0.700 CausalMutation CLINVAR DVL3 Alleles Resulting in a -1 Frameshift of the Last Exon Mediate Autosomal-Dominant Robinow Syndrome. 26924530 2016
dbSNP: rs869025218
rs869025218
Entrez Id: 1857
Gene Symbol: DVL3
DVL3
CUI: C4551475
Disease:
ROBINOW SYNDROME, AUTOSOMAL DOMINANT 1
G 0.700 CausalMutation CLINVAR DVL3 Alleles Resulting in a -1 Frameshift of the Last Exon Mediate Autosomal-Dominant Robinow Syndrome. 26924530 2016
dbSNP: rs869025219
rs869025219
Entrez Id: 1857
Gene Symbol: DVL3
DVL3
CUI: C4551475
Disease:
ROBINOW SYNDROME, AUTOSOMAL DOMINANT 1
G 0.700 CausalMutation CLINVAR DVL3 Alleles Resulting in a -1 Frameshift of the Last Exon Mediate Autosomal-Dominant Robinow Syndrome. 26924530 2016
dbSNP: rs1553811652
rs1553811652
Entrez Id: 1857
Gene Symbol: DVL3
DVL3
CUI: C4225363
Disease:
ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2
A 0.700 GeneticVariation CLINVAR
dbSNP: rs869025215
rs869025215
Entrez Id: 1857
Gene Symbol: DVL3
DVL3
CUI: C4225164
Disease:
ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3
C 0.700 CausalMutation CLINVAR
dbSNP: rs869025216
rs869025216
Entrez Id: 1857
Gene Symbol: DVL3
DVL3
CUI: C4225164
Disease:
ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3
G 0.700 CausalMutation CLINVAR
dbSNP: rs869025217
rs869025217
Entrez Id: 1857
Gene Symbol: DVL3
DVL3
CUI: C4225164
Disease:
ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3
A 0.700 CausalMutation CLINVAR
dbSNP: rs869025218
rs869025218
Entrez Id: 1857
Gene Symbol: DVL3
DVL3
CUI: C4225164
Disease:
ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3
G 0.700 CausalMutation CLINVAR
dbSNP: rs869025219
rs869025219
Entrez Id: 1857
Gene Symbol: DVL3
DVL3
CUI: C4225164
Disease:
ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3
G 0.700 CausalMutation CLINVAR