rs1553404283
|
Entrez Id: |
7840 |
Gene Symbol: |
ALMS1 |
ALMS1
|
Alstrom Syndrome
|
C |
0.700 |
CausalMutation |
CLINVAR |
Diffuse left ventricular interstitial fibrosis is associated with sub-clinical myocardial dysfunction in Alström Syndrome: an observational study.
|
26104972 |
2015 |
rs1553404358
|
Entrez Id: |
7840 |
Gene Symbol: |
ALMS1 |
ALMS1
|
Alstrom Syndrome
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Diffuse left ventricular interstitial fibrosis is associated with sub-clinical myocardial dysfunction in Alström Syndrome: an observational study.
|
26104972 |
2015 |
rs769291842
|
Entrez Id: |
7840 |
Gene Symbol: |
ALMS1 |
ALMS1
|
Alstrom Syndrome
|
TA |
0.700 |
GeneticVariation |
CLINVAR |
Diffuse left ventricular interstitial fibrosis is associated with sub-clinical myocardial dysfunction in Alström Syndrome: an observational study.
|
26104972 |
2015 |
rs777476179
|
Entrez Id: |
7840 |
Gene Symbol: |
ALMS1 |
ALMS1
|
Alstrom Syndrome
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Diffuse left ventricular interstitial fibrosis is associated with sub-clinical myocardial dysfunction in Alström Syndrome: an observational study.
|
26104972 |
2015 |
rs1553404066
|
Entrez Id: |
7840 |
Gene Symbol: |
ALMS1 |
ALMS1
|
Alstrom Syndrome
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Comprehensive Molecular Diagnosis of a Large Chinese Leber Congenital Amaurosis Cohort.
|
26047050 |
2015 |
rs1553404109
|
Entrez Id: |
7840 |
Gene Symbol: |
ALMS1 |
ALMS1
|
Alstrom Syndrome
|
AT |
0.700 |
CausalMutation |
CLINVAR |
ALMS1 null mutations: a common cause of Leber congenital amaurosis and early-onset severe cone-rod dystrophy.
|
26010121 |
2016 |
rs755616266
|
Entrez Id: |
7840 |
Gene Symbol: |
ALMS1 |
ALMS1
|
Alstrom Syndrome
|
C |
0.700 |
CausalMutation |
CLINVAR |
ALMS1 null mutations: a common cause of Leber congenital amaurosis and early-onset severe cone-rod dystrophy.
|
26010121 |
2016 |
rs779366889
|
Entrez Id: |
7840 |
Gene Symbol: |
ALMS1 |
ALMS1
|
Alstrom Syndrome
|
C |
0.700 |
CausalMutation |
CLINVAR |
ALMS1 null mutations: a common cause of Leber congenital amaurosis and early-onset severe cone-rod dystrophy.
|
26010121 |
2016 |
rs1275113273
|
Entrez Id: |
7840 |
Gene Symbol: |
ALMS1 |
ALMS1
|
Alstrom Syndrome
|
T |
0.700 |
CausalMutation |
CLINVAR |
Alström Syndrome: Mutation Spectrum of ALMS1.
|
25846608 |
2015 |
rs1370417967
|
Entrez Id: |
7840 |
Gene Symbol: |
ALMS1 |
ALMS1
|
Alstrom Syndrome
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Alström Syndrome: Mutation Spectrum of ALMS1.
|
25846608 |
2015 |
rs1476205467
|
Entrez Id: |
7840 |
Gene Symbol: |
ALMS1 |
ALMS1
|
Alstrom Syndrome
|
A |
0.700 |
CausalMutation |
CLINVAR |
Alström Syndrome: Mutation Spectrum of ALMS1.
|
25846608 |
2015 |
rs1553403282
|
Entrez Id: |
7840 |
Gene Symbol: |
ALMS1 |
ALMS1
|
Alstrom Syndrome
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Alström Syndrome: Mutation Spectrum of ALMS1.
|
25846608 |
2015 |
rs1553404252
|
Entrez Id: |
7840 |
Gene Symbol: |
ALMS1 |
ALMS1
|
Alstrom Syndrome
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Alström Syndrome: Mutation Spectrum of ALMS1.
|
25846608 |
2015 |
rs1553404358
|
Entrez Id: |
7840 |
Gene Symbol: |
ALMS1 |
ALMS1
|
Alstrom Syndrome
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Alström Syndrome: Mutation Spectrum of ALMS1.
|
25846608 |
2015 |
rs1553409691
|
Entrez Id: |
7840 |
Gene Symbol: |
ALMS1 |
ALMS1
|
Alstrom Syndrome
|
CT |
0.700 |
GeneticVariation |
CLINVAR |
Alström Syndrome: Mutation Spectrum of ALMS1.
|
25846608 |
2015 |
rs1553409710
|
Entrez Id: |
7840 |
Gene Symbol: |
ALMS1 |
ALMS1
|
Alstrom Syndrome
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Alström Syndrome: Mutation Spectrum of ALMS1.
|
25846608 |
2015 |
rs1553421626
|
Entrez Id: |
7840 |
Gene Symbol: |
ALMS1 |
ALMS1
|
Alstrom Syndrome
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Alström Syndrome: Mutation Spectrum of ALMS1.
|
25846608 |
2015 |
rs387906312
|
Entrez Id: |
7840 |
Gene Symbol: |
ALMS1 |
ALMS1
|
Alstrom Syndrome
|
A |
0.700 |
CausalMutation |
CLINVAR |
Alström Syndrome: Mutation Spectrum of ALMS1.
|
25846608 |
2015 |
rs747272625
|
Entrez Id: |
7840 |
Gene Symbol: |
ALMS1 |
ALMS1
|
Alstrom Syndrome
|
T |
0.700 |
CausalMutation |
CLINVAR |
Alström Syndrome: Mutation Spectrum of ALMS1.
|
25846608 |
2015 |
rs757722767
|
Entrez Id: |
7840 |
Gene Symbol: |
ALMS1 |
ALMS1
|
Alstrom Syndrome
|
GA |
0.700 |
GeneticVariation |
CLINVAR |
Alström Syndrome: Mutation Spectrum of ALMS1.
|
25846608 |
2015 |
rs759603306
|
Entrez Id: |
7840 |
Gene Symbol: |
ALMS1 |
ALMS1
|
Alstrom Syndrome
|
AAT |
0.700 |
CausalMutation |
CLINVAR |
Alström Syndrome: Mutation Spectrum of ALMS1.
|
25846608 |
2015 |
rs760264695
|
Entrez Id: |
7840 |
Gene Symbol: |
ALMS1 |
ALMS1
|
Alstrom Syndrome
|
TGTTA |
0.700 |
CausalMutation |
CLINVAR |
Alström Syndrome: Mutation Spectrum of ALMS1.
|
25846608 |
2015 |
rs770558150
|
Entrez Id: |
7840 |
Gene Symbol: |
ALMS1 |
ALMS1
|
Alstrom Syndrome
|
T |
0.700 |
CausalMutation |
CLINVAR |
Alström Syndrome: Mutation Spectrum of ALMS1.
|
25846608 |
2015 |
rs772136379
|
Entrez Id: |
7840 |
Gene Symbol: |
ALMS1 |
ALMS1
|
Alstrom Syndrome
|
G |
0.700 |
CausalMutation |
CLINVAR |
Alström Syndrome: Mutation Spectrum of ALMS1.
|
25846608 |
2015 |
rs779366889
|
Entrez Id: |
7840 |
Gene Symbol: |
ALMS1 |
ALMS1
|
Alstrom Syndrome
|
C |
0.700 |
CausalMutation |
CLINVAR |
Alström Syndrome: Mutation Spectrum of ALMS1.
|
25846608 |
2015 |