rs80338859
|
|
Smith-Lemli-Opitz Syndrome
|
A |
0.850 |
CausalMutation
|
CLINVAR |
A placebo-controlled trial of simvastatin therapy in Smith-Lemli-Opitz syndrome.
|
27513191 |
2017 |
rs80338859
|
|
Smith-Lemli-Opitz Syndrome
|
A |
0.850 |
CausalMutation
|
CLINVAR |
The results of our previous newborn screening, based on the carrier frequency of the two most common SLOS-causing mutations in Poland (p.W151X and p.V326L), would make SLOS one of the most frequent recessive disorders in our country (with an incidence of 1:2,300 - 1:3,937).
|
20556518 |
2010 |
rs80338859
|
|
Smith-Lemli-Opitz Syndrome
|
A |
0.850 |
CausalMutation
|
CLINVAR |
DHCR7 mutations and genotype-phenotype correlation in 37 Polish patients with Smith-Lemli-Opitz syndrome.
|
15521979 |
2004 |
rs80338859
|
|
Smith-Lemli-Opitz Syndrome
|
A |
0.850 |
CausalMutation
|
CLINVAR |
Smith-Lemli-Opitz syndrome: molecular-genetic analysis of ten families.
|
10896306 |
2000 |
rs80338859
|
|
Smith-Lemli-Opitz Syndrome
|
A |
0.850 |
CausalMutation
|
CLINVAR |
Spectrum of Delta(7)-dehydrocholesterol reductase mutations in patients with the Smith-Lemli-Opitz (RSH) syndrome.
|
10814720 |
2000 |
rs80338859
|
|
Smith-Lemli-Opitz Syndrome
|
A |
0.850 |
CausalMutation
|
CLINVAR |
Among the mutations found in patients with the SLOS, are missense (P51S, T93M, L99P, L157P, A247V, V326L, R352W, C380S, R404C, and G410S), nonsense (W151X), and splice site (IVS8-1G>C) mutations as well as an out of frame deletion (720-735 del).
|
9653161 |
1998 |
rs80338853
|
|
Smith-Lemli-Opitz Syndrome
|
A |
0.840 |
CausalMutation
|
CLINVAR |
High frequency of p.Thr93Met in Smith-Lemli-Opitz syndrome patients in Turkey.
|
22211794 |
2012 |
rs80338853
|
|
Smith-Lemli-Opitz Syndrome
|
A |
0.840 |
CausalMutation
|
CLINVAR |
The analysis included 20 Spanish and 12 Italian SLOS patients and revealed very different mutation spectra in these patients compared to previously described patients from Czechoslovakia, Germany, Poland, and the UK and implicated p.Thr93Met on the J haplotype as the most frequent Mediterranean founder mutation.
|
15776424 |
2005 |
rs80338853
|
|
Smith-Lemli-Opitz Syndrome
|
A |
0.840 |
CausalMutation
|
CLINVAR |
3beta-hydroxysterol Delta7-reductase and the Smith-Lemli-Opitz syndrome.
|
15670717 |
2005 |
rs80338853
|
|
Smith-Lemli-Opitz Syndrome
|
A |
0.840 |
CausalMutation
|
CLINVAR |
Founder effect for the T93M DHCR7 mutation in Smith-Lemli-Opitz syndrome.
|
14981719 |
2004 |
rs80338853
|
|
Smith-Lemli-Opitz Syndrome
|
A |
0.840 |
CausalMutation
|
CLINVAR |
We also report rapid polymerase chain reaction (PCR)-based assays developed to detect four of the recurring mutations (T93M, W151X, V326L, and R404C) and six other RSH/SLOS mutations (321G-->C, L109P, T154M, T289I, Y318N, and L341P).
|
10995508 |
2000 |
rs80338853
|
|
Smith-Lemli-Opitz Syndrome
|
A |
0.840 |
CausalMutation
|
CLINVAR |
Mutational spectrum in the Delta7-sterol reductase gene and genotype-phenotype correlation in 84 patients with Smith-Lemli-Opitz syndrome.
|
10677299 |
2000 |
rs80338853
|
|
Smith-Lemli-Opitz Syndrome
|
A |
0.840 |
CausalMutation
|
CLINVAR |
Smith-Lemli-Opitz syndrome: evidence of T93M as a common mutation of delta7-sterol reductase in Italy and report of three novel mutations.
|
10602371 |
1999 |
rs80338853
|
|
Smith-Lemli-Opitz Syndrome
|
A |
0.840 |
CausalMutation
|
CLINVAR |
Among the mutations found in patients with the SLOS, are missense (P51S, T93M, L99P, L157P, A247V, V326L, R352W, C380S, R404C, and G410S), nonsense (W151X), and splice site (IVS8-1G>C) mutations as well as an out of frame deletion (720-735 del).
|
9653161 |
1998 |
rs80338853
|
|
Smith-Lemli-Opitz Syndrome
|
A |
0.840 |
GeneticVariation
|
CLINVAR |
|
|
|
rs121909768
|
|
Smith-Lemli-Opitz Syndrome
|
T |
0.810 |
CausalMutation
|
CLINVAR |
Smith-Lemli-Opitz syndrome among Arabs.
|
21696385 |
2012 |
rs121909768
|
|
Smith-Lemli-Opitz Syndrome
|
T |
0.810 |
CausalMutation
|
CLINVAR |
Differences between predicted and established diagnoses of Smith-Lemli-Opitz syndrome in the Polish population: underdiagnosis or loss of affected fetuses?
|
20556518 |
2010 |
rs121909768
|
|
Smith-Lemli-Opitz Syndrome
|
T |
0.810 |
CausalMutation
|
CLINVAR |
Prenatal diagnosis of Smith-Lemli-Opitz syndrome (SLOS) by DHCR7 mutation analysis.
|
17441222 |
2007 |
rs121909768
|
|
Smith-Lemli-Opitz Syndrome
|
T |
0.810 |
CausalMutation
|
CLINVAR |
These results suggest that R352Q is a predominant founder mutation in Japanese SLOS patients.
|
16044199 |
2005 |
rs121909768
|
|
Smith-Lemli-Opitz Syndrome
|
T |
0.810 |
CausalMutation
|
CLINVAR |
Mutational spectrum in the Delta7-sterol reductase gene and genotype-phenotype correlation in 84 patients with Smith-Lemli-Opitz syndrome.
|
10677299 |
2000 |
rs61757582
|
|
Smith-Lemli-Opitz Syndrome
|
A |
0.810 |
CausalMutation
|
CLINVAR |
Smith-Lemli-Opitz syndrome: Objective assessment of facial phenotype.
|
22438180 |
2012 |
rs61757582
|
|
Smith-Lemli-Opitz Syndrome
|
A |
0.810 |
CausalMutation
|
CLINVAR |
Identification of nine novel DHCR7 missense mutations in patients with Smith-Lemli-Opitz syndrome (SLOS).
|
15954111 |
2005 |
rs61757582
|
|
Smith-Lemli-Opitz Syndrome
|
A |
0.810 |
CausalMutation
|
CLINVAR |
Residual cholesterol synthesis and simvastatin induction of cholesterol synthesis in Smith-Lemli-Opitz syndrome fibroblasts.
|
15896653 |
2005 |
rs61757582
|
|
Smith-Lemli-Opitz Syndrome
|
A |
0.810 |
CausalMutation
|
CLINVAR |
[Clinical characteristics and diagnosis of Smith-Lemli-Opitz syndrome and tentative phenotype-genotype correlation: report of 45 cases].
|
12818773 |
2003 |
rs61757582
|
|
Smith-Lemli-Opitz Syndrome
|
A |
0.810 |
CausalMutation
|
CLINVAR |
Mutational spectrum in the Delta7-sterol reductase gene and genotype-phenotype correlation in 84 patients with Smith-Lemli-Opitz syndrome.
|
10677299 |
2000 |