rs4149056
|
|
|
0.020 |
GeneticVariation |
BEFREE |
No association of the SLCO1B1 rs2306283 and rs4149056 genotypes or haplotypes with the presence of myalgia or creatine kinase (CK) values was found.
|
21928084 |
2012 |
rs4149056
|
|
|
0.020 |
GeneticVariation |
BEFREE |
We evaluated the effect of rs4363657 and rs4149056 in SLCO1B1, which encodes organic anion-transporting polypeptide OATP1B1, a regulator of hepatic statin uptake, on clinically reported myalgia.
|
23708174 |
2013 |
rs61752717
|
|
|
0.020 |
GeneticVariation |
BEFREE |
Acute orchitis and protracted febrile myalgia as rare clinical findings were more common in M694V homozygotes.
|
22057232 |
2012 |
rs61752717
|
|
|
0.020 |
GeneticVariation |
BEFREE |
Group 1 had significantly higher rate of myalgia, arthritis/arthralgia, erysipelas like erythema, amyloidosis, protracted febrile myalgia and M694V mutation compared with Group 2.
|
25669438 |
2015 |
rs1048379601
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Here we report on a 4-year-old girl presenting with myalgia and muscle cramps due to a caveolin-3 deficiency in her dystrophic skeletal muscle as a result of a heterozygous 136G-->A substitution in the caveolin-3 gene.
|
11001938 |
2000 |
rs116840789
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Here we report on a 4-year-old girl presenting with myalgia and muscle cramps due to a caveolin-3 deficiency in her dystrophic skeletal muscle as a result of a heterozygous 136G-->A substitution in the caveolin-3 gene.
|
11001938 |
2000 |
rs1187636039
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In the family assessed, the p.D294E mutation segregated in association with a particular sensitivity to cold exposure (especially arthralgias and myalgia), but not always with an inflammatory phenotype (e.g., urticarial rash or fever).
|
21360512 |
2011 |
rs1263071018
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Here we report on a 4-year-old girl presenting with myalgia and muscle cramps due to a caveolin-3 deficiency in her dystrophic skeletal muscle as a result of a heterozygous 136G-->A substitution in the caveolin-3 gene.
|
11001938 |
2000 |
rs12722
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We found that COL1A1 (minor) T-allele carriers ( rs1800012 ) and (major) T-allele homozygotes ( rs2249492 ) were generally weaker ( P ≤ 0.019); and (minor) A-allele carriers of COL2A1 ( P = 0.002) and (major) T-allele carriers of COL5A1 ( P = 0.004) SNPs reported greater muscle soreness, all compared with their respective major ( rs1800012 ; rs2070739 ) and minor ( rs2249492 ; rs12722 ) allele homozygote counterparts.
|
29799806 |
2018 |
rs147080557
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In the family assessed, the p.D294E mutation segregated in association with a particular sensitivity to cold exposure (especially arthralgias and myalgia), but not always with an inflammatory phenotype (e.g., urticarial rash or fever).
|
21360512 |
2011 |
rs1800012
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We found that COL1A1 (minor) T-allele carriers ( rs1800012 ) and (major) T-allele homozygotes ( rs2249492 ) were generally weaker ( P ≤ 0.019); and (minor) A-allele carriers of COL2A1 ( P = 0.002) and (major) T-allele carriers of COL5A1 ( P = 0.004) SNPs reported greater muscle soreness, all compared with their respective major ( rs1800012 ; rs2070739 ) and minor ( rs2249492 ; rs12722 ) allele homozygote counterparts.
|
29799806 |
2018 |
rs2249492
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We found that COL1A1 (minor) T-allele carriers ( rs1800012 ) and (major) T-allele homozygotes ( rs2249492 ) were generally weaker ( P ≤ 0.019); and (minor) A-allele carriers of COL2A1 ( P = 0.002) and (major) T-allele carriers of COL5A1 ( P = 0.004) SNPs reported greater muscle soreness, all compared with their respective major ( rs1800012 ; rs2070739 ) and minor ( rs2249492 ; rs12722 ) allele homozygote counterparts.
|
29799806 |
2018 |
rs2306283
|
|
|
0.010 |
GeneticVariation |
BEFREE |
No association of the SLCO1B1 rs2306283 and rs4149056 genotypes or haplotypes with the presence of myalgia or creatine kinase (CK) values was found.
|
21928084 |
2012 |
rs4363657
|
|
|
0.010 |
GeneticVariation |
BEFREE |
SLCO1B1 tagging rs4363657 polymorphism was analyzed in 2 groups of patients with dyslipidemia (treated with simvastatin or atorvastatin, 10 or 20 mg per day), subgroup with statin-induced myalgia (N=286), and subgroup (N=707) without myalgia/myopathy, and in 2301 population controls without lipid-lowering treatment.
|
25992810 |
2015 |
rs759411064
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Here we report on a 4-year-old girl presenting with myalgia and muscle cramps due to a caveolin-3 deficiency in her dystrophic skeletal muscle as a result of a heterozygous 136G-->A substitution in the caveolin-3 gene.
|
11001938 |
2000 |
rs7924316
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We found that men who were 1) homozygous for the rare IGF-II C13790G allele and rare allele for the ApaI (G17200A) SNP demonstrated the greatest strength loss immediately after exercise, greatest soreness, and highest postexercise serum CK activity; 2) homozygous wild type for IGF2AS (G11711T, rs7924316) had the greatest strength loss and most muscle soreness; and 3) homozygous wild type for the IGF2AS G11711T SNP showed the greatest strength loss, highest muscle soreness, and greater CK and myoglobin response to exercise.
|
17289909 |
2007 |
rs138977195
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs878855327
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs121918459
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs776974834
|
|
G |
0.700 |
SusceptibilityMutation |
CLINVAR |
|
|
|
rs781565158
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1555876283
|
|
T |
0.700 |
SusceptibilityMutation |
CLINVAR |
|
|
|
rs1569548274
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs398123383
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|