RBM10, RNA binding motif protein 10, 8241

N. diseases: 99; N. variants: 8
Disease: TARP syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1556770954
rs1556770954
Entrez Id: 8241
Gene Symbol: RBM10
RBM10
CUI: C1839463
Disease:
TARP syndrome 		G 0.700 CausalMutation CLINVAR Long-term survival in TARP syndrome and confirmation of RBM10 as the disease-causing gene. 21910224 2011
dbSNP: rs1556770954
rs1556770954
Entrez Id: 8241
Gene Symbol: RBM10
RBM10
CUI: C1839463
Disease:
TARP syndrome 		G 0.700 CausalMutation CLINVAR Massively parallel sequencing of exons on the X chromosome identifies RBM10 as the gene that causes a syndromic form of cleft palate. 20451169 2010
dbSNP: rs1556778986
rs1556778986
Entrez Id: 8241
Gene Symbol: RBM10
RBM10
CUI: C1839463
Disease:
TARP syndrome 		A 0.700 CausalMutation CLINVAR
dbSNP: rs267607000
rs267607000
Entrez Id: 8241
Gene Symbol: RBM10
RBM10
CUI: C1839463
Disease:
TARP syndrome 		A 0.700 CausalMutation CLINVAR
dbSNP: rs886044715
rs886044715
Entrez Id: 8241
Gene Symbol: RBM10
RBM10
CUI: C1839463
Disease:
TARP syndrome 		CA 0.700 CausalMutation CLINVAR
dbSNP: rs886044718
rs886044718
Entrez Id: 8241
Gene Symbol: RBM10
RBM10
CUI: C1839463
Disease:
TARP syndrome 		T 0.700 CausalMutation CLINVAR