SMO, smoothened, frizzled class receptor, 6608

N. diseases: 215; N. variants: 13
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs879255280
rs879255280
Entrez Id: 6608
Gene Symbol: SMO
SMO
CUI: C0549629
Disease:
Abnormal delivery
T 0.700 CausalMutation CLINVAR
dbSNP: rs879255280
rs879255280
Entrez Id: 6608
Gene Symbol: SMO
SMO
CUI: C0278876
Disease:
Adult Medulloblastoma
0.010 GeneticVariation BEFREE Medulloblastoma in a Patient with Curry-Jones Syndrome with a mosaic variant, c.1234C > T (p.Leu412Phe), in SMO. 31825089 2020
dbSNP: rs121918347
rs121918347
Entrez Id: 6608
Gene Symbol: SMO
SMO
CUI: C3838465
Disease:
BASAL CELL CARCINOMA, SOMATIC
T 0.700 CausalMutation CLINVAR
dbSNP: rs121918348
rs121918348
Entrez Id: 6608
Gene Symbol: SMO
SMO
CUI: C3838465
Disease:
BASAL CELL CARCINOMA, SOMATIC
A 0.700 CausalMutation CLINVAR
dbSNP: rs121918347
rs121918347
Entrez Id: 6608
Gene Symbol: SMO
SMO
CUI: C4721806
Disease:
Carcinoma, Basal Cell
0.700 GeneticVariation UNIPROT
dbSNP: rs121918348
rs121918348
Entrez Id: 6608
Gene Symbol: SMO
SMO
CUI: C4721806
Disease:
Carcinoma, Basal Cell
0.700 GeneticVariation UNIPROT
dbSNP: rs17710891
rs17710891
Entrez Id: 6608
Gene Symbol: SMO
SMO
CUI: C4721806
Disease:
Carcinoma, Basal Cell
C 0.700 CausalMutation CLINVAR Smoothened variants explain the majority of drug resistance in basal cell carcinoma. 25759020 2015
dbSNP: rs17710891
rs17710891
Entrez Id: 6608
Gene Symbol: SMO
SMO
CUI: C4721806
Disease:
Carcinoma, Basal Cell
C 0.700 CausalMutation CLINVAR Vismodegib. 22679179 2012
dbSNP: rs17710891
rs17710891
Entrez Id: 6608
Gene Symbol: SMO
SMO
CUI: C4721806
Disease:
Carcinoma, Basal Cell
C 0.700 CausalMutation CLINVAR Smoothened mutation confers resistance to a Hedgehog pathway inhibitor in medulloblastoma. 19726788 2009
dbSNP: rs879255280
rs879255280
Entrez Id: 6608
Gene Symbol: SMO
SMO
CUI: C4721806
Disease:
Carcinoma, Basal Cell
T 0.700 CausalMutation CLINVAR
dbSNP: rs41303402
rs41303402
Entrez Id: 6608
Gene Symbol: SMO
SMO
CUI: C4721806
Disease:
Carcinoma, Basal Cell
0.010 GeneticVariation BEFREE Other genotypes, such as the TT in SHH rs104894049 331 A/T and the GG in SMO rs41303402 385 G/A also statistically raised the risk of BCC, but these associations were weaker. 26590974 2016
dbSNP: rs41303402
rs41303402
Entrez Id: 6608
Gene Symbol: SMO
SMO
CUI: C4721806
Disease:
Carcinoma, Basal Cell
0.010 GeneticVariation BEFREE Other genotypes, such as the TT in SHH rs104894049 331 A/T and the GG in SMO rs41303402 385 G/A also statistically raised the risk of BCC, but these associations were weaker. 26590974 2016
dbSNP: rs912880810
rs912880810
Entrez Id: 6608
Gene Symbol: SMO
SMO
CUI: C4721806
Disease:
Carcinoma, Basal Cell
0.010 GeneticVariation BEFREE These results mainly underline the potential role of SHH3 rs104894040 349 T/C gene polymorphism in the development of skin basal cell carcinomas in patients of Polish origin. 26590974 2016
dbSNP: rs778791846
rs778791846
Entrez Id: 6608
Gene Symbol: SMO
SMO
CUI: C0086543
Disease:
Cataract
0.010 GeneticVariation BEFREE Here we reported the first identification of compound heterozygous mutations (c.G338A; p.R113Q and c.C1619T; p.A540V) in the SMO gene in a patient with both anterior segment dysgenesis (congenital corneal opacity, cataract) and morning glory syndrome, using trio-based whole exome sequencing. 31301482 2019
dbSNP: rs879255280
rs879255280
Entrez Id: 6608
Gene Symbol: SMO
SMO
CUI: C0278510
Disease:
Childhood Medulloblastoma
0.010 GeneticVariation BEFREE Medulloblastoma in a Patient with Curry-Jones Syndrome with a mosaic variant, c.1234C > T (p.Leu412Phe), in SMO. 31825089 2020
dbSNP: rs578002520
rs578002520
Entrez Id: 6608
Gene Symbol: SMO
SMO
CUI: C0344535
Disease:
Congenital corneal opacity
0.010 GeneticVariation BEFREE Here we reported the first identification of compound heterozygous mutations (c.G338A; p.R113Q and c.C1619T; p.A540V) in the SMO gene in a patient with both anterior segment dysgenesis (congenital corneal opacity, cataract) and morning glory syndrome, using trio-based whole exome sequencing. 31301482 2019
dbSNP: rs778791846
rs778791846
Entrez Id: 6608
Gene Symbol: SMO
SMO
CUI: C0344535
Disease:
Congenital corneal opacity
0.010 GeneticVariation BEFREE Here we reported the first identification of compound heterozygous mutations (c.G338A; p.R113Q and c.C1619T; p.A540V) in the SMO gene in a patient with both anterior segment dysgenesis (congenital corneal opacity, cataract) and morning glory syndrome, using trio-based whole exome sequencing. 31301482 2019
dbSNP: rs879255280
rs879255280
Entrez Id: 6608
Gene Symbol: SMO
SMO
CUI: C4020699
Disease:
Congenital dermal melanocytosis
T 0.700 CausalMutation CLINVAR
dbSNP: rs879255280
rs879255280
Entrez Id: 6608
Gene Symbol: SMO
SMO
CUI: C4014479
Disease:
CULLER-JONES SYNDROME
0.010 GeneticVariation BEFREE A recurrent, mosaic mutation of SMO (c.1234 C>T; p.Leu412Phe) causes CJS. 28386950 2017
dbSNP: rs1061280
rs1061280
Entrez Id: 6608
Gene Symbol: SMO
SMO
CUI: C0014868
Disease:
Esophagitis
0.010 GeneticVariation BEFREE Patients with the AG+GG genotype of SMO:rs1061280 had an 81% reduced risk of developing esophagitis (OR: 0.19, 95% CI: 0.07-0.53, p = 0.001, q = 0.06). 26991123 2016
dbSNP: rs1061285
rs1061285
Entrez Id: 6608
Gene Symbol: SMO
SMO
CUI: C0014868
Disease:
Esophagitis
0.010 GeneticVariation BEFREE After multiple comparison correction, RPS6KB2:rs10274, SMO:rs1061280, SMO:rs1061285 remained significantly associated with esophagitis, while processing gene DGCR8:rs720014, DGCR8:rs3757, DGCR8:rs1633445 remained significantly associated with pneumonitis. 26991123 2016
dbSNP: rs41303402
rs41303402
Entrez Id: 6608
Gene Symbol: SMO
SMO
CUI: C3811653
Disease:
Experimental Organism Basal Cell Carcinoma
0.010 GeneticVariation BEFREE Other genotypes, such as the TT in SHH rs104894049 331 A/T and the GG in SMO rs41303402 385 G/A also statistically raised the risk of BCC, but these associations were weaker. 26590974 2016
dbSNP: rs41303402
rs41303402
Entrez Id: 6608
Gene Symbol: SMO
SMO
CUI: C3811653
Disease:
Experimental Organism Basal Cell Carcinoma
0.010 GeneticVariation BEFREE Other genotypes, such as the TT in SHH rs104894049 331 A/T and the GG in SMO rs41303402 385 G/A also statistically raised the risk of BCC, but these associations were weaker. 26590974 2016
dbSNP: rs912880810
rs912880810
Entrez Id: 6608
Gene Symbol: SMO
SMO
CUI: C3811653
Disease:
Experimental Organism Basal Cell Carcinoma
0.010 GeneticVariation BEFREE The presence of CC genotype in the SHH rs104894040 349 T/C polymorphism was linked to the highest risk of BCC development (OR 87.9, p < 0.001). 26590974 2016
dbSNP: rs879255280
rs879255280
Entrez Id: 6608
Gene Symbol: SMO
SMO
CUI: C0018552
Disease:
Hamartoma
T 0.700 CausalMutation CLINVAR