rs118204016
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs121908545
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Exome sequencing in Jewish and Arab patients with rhabdomyolysis reveals single-gene etiology in 43% of cases.
|
28779239 |
2017 |
rs121918608
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Exome sequencing in Jewish and Arab patients with rhabdomyolysis reveals single-gene etiology in 43% of cases.
|
28779239 |
2017 |
rs138058572
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs1555735545
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1555762532
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Exome sequencing in Jewish and Arab patients with rhabdomyolysis reveals single-gene etiology in 43% of cases.
|
28779239 |
2017 |
rs202143236
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Exome sequencing in Jewish and Arab patients with rhabdomyolysis reveals single-gene etiology in 43% of cases.
|
28779239 |
2017 |
rs28937900
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs74315294
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Exome sequencing in Jewish and Arab patients with rhabdomyolysis reveals single-gene etiology in 43% of cases.
|
28779239 |
2017 |
rs750422335
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Exome sequencing in Jewish and Arab patients with rhabdomyolysis reveals single-gene etiology in 43% of cases.
|
28779239 |
2017 |
rs751995154
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs752298579
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Recurrent Muscle Weakness with Rhabdomyolysis, Metabolic Crises, and Cardiac Arrhythmia Due to Bi-allelic TANGO2 Mutations.
|
26805781 |
2016 |
rs763794604
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Exome sequencing in Jewish and Arab patients with rhabdomyolysis reveals single-gene etiology in 43% of cases.
|
28779239 |
2017 |
rs867410737
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Biallelic Mutations in ATP5F1D, which Encodes a Subunit of ATP Synthase, Cause a Metabolic Disorder.
|
29478781 |
2018 |
rs2819742
|
|
G |
0.700 |
GeneticVariation |
GWASCAT |
Cerivastatin, genetic variants, and the risk of rhabdomyolysis.
|
21386754 |
2011 |