Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121918349
rs121918349
Entrez Id: 7480
Gene Symbol: WNT10B
WNT10B
CUI: C2749665
Disease:
SPLIT-HAND/FOOT MALFORMATION 6 (disorder)
0.800 GeneticVariation UNIPROT Homozygous WNT10b mutation and complex inheritance in Split-Hand/Foot Malformation. 18515319 2008
dbSNP: rs121918349
rs121918349
Entrez Id: 7480
Gene Symbol: WNT10B
WNT10B
CUI: C2749665
Disease:
SPLIT-HAND/FOOT MALFORMATION 6 (disorder)
A 0.800 CausalMutation CLINVAR