rs1242078669
×
Entrez Id:
667
Gene Symbol:
DST
DST
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI
A
0.700
GeneticVariation
CLINVAR
rs1330945347
×
Entrez Id:
667
Gene Symbol:
DST
DST
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI
T
0.700
GeneticVariation
CLINVAR
rs1562435373
×
Entrez Id:
667
Gene Symbol:
DST
DST
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI
A
0.700
GeneticVariation
CLINVAR
rs201871537
DST;DST-AS1
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI
T
0.700
GeneticVariation
CLINVAR
rs398122819
×
Entrez Id:
667
Gene Symbol:
DST
DST
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI
C
0.700
CausalMutation
CLINVAR
rs398122943
×
Entrez Id:
667
Gene Symbol:
DST
DST
EPIDERMOLYSIS BULLOSA SIMPLEX, AUTOSOMAL RECESSIVE 2
A
0.700
CausalMutation
CLINVAR
rs577972555
×
Entrez Id:
667
Gene Symbol:
DST
DST
EPIDERMOLYSIS BULLOSA SIMPLEX, AUTOSOMAL RECESSIVE 2
A
0.700
CausalMutation
CLINVAR
rs577972555
×
Entrez Id:
667
Gene Symbol:
DST
DST
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI
A
0.700
CausalMutation
CLINVAR
rs748899221
×
Entrez Id:
667
Gene Symbol:
DST
DST
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI
G
0.700
CausalMutation
CLINVAR
rs748899221
×
Entrez Id:
667
Gene Symbol:
DST
DST
EPIDERMOLYSIS BULLOSA SIMPLEX, AUTOSOMAL RECESSIVE 2
G
0.700
CausalMutation
CLINVAR
rs759006806
×
Entrez Id:
667
Gene Symbol:
DST
DST
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI
CT
0.700
CausalMutation
CLINVAR
rs770035646
×
Entrez Id:
667
Gene Symbol:
DST
DST
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI
A
0.700
CausalMutation
CLINVAR
rs770035646
×
Entrez Id:
667
Gene Symbol:
DST
DST
EPIDERMOLYSIS BULLOSA SIMPLEX, AUTOSOMAL RECESSIVE 2
A
0.700
CausalMutation
CLINVAR
rs778397331
×
Entrez Id:
667
Gene Symbol:
DST
DST
EPIDERMOLYSIS BULLOSA SIMPLEX, AUTOSOMAL RECESSIVE 2
A
0.700
CausalMutation
CLINVAR
rs778397331
×
Entrez Id:
667
Gene Symbol:
DST
DST
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI
A
0.700
CausalMutation
CLINVAR
rs201045495
×
Entrez Id:
667
Gene Symbol:
DST
DST
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI
A
0.700
CausalMutation
CLINVAR
A homozygous nonsense mutation within the dystonin gene coding for the coiled-coil domain of the epithelial isoform of BPAG1 underlies a new subtype of autosomal recessive epidermolysis bullosa simplex.
20164846
2010
rs201045495
×
Entrez Id:
667
Gene Symbol:
DST
DST
EPIDERMOLYSIS BULLOSA SIMPLEX, AUTOSOMAL RECESSIVE 2
A
0.700
CausalMutation
CLINVAR
A homozygous nonsense mutation within the dystonin gene coding for the coiled-coil domain of the epithelial isoform of BPAG1 underlies a new subtype of autosomal recessive epidermolysis bullosa simplex.
20164846
2010
rs9475752
×
Entrez Id:
667
Gene Symbol:
DST
DST
Age at menarche
C
0.700
GeneticVariation
GWASCAT
Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche.
25231870
2014
rs201045495
×
Entrez Id:
667
Gene Symbol:
DST
DST
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI
A
0.700
CausalMutation
CLINVAR
Founder mutation in dystonin-e underlying autosomal recessive epidermolysis bullosa simplex in Kuwait.
25059916
2015
rs201045495
×
Entrez Id:
667
Gene Symbol:
DST
DST
EPIDERMOLYSIS BULLOSA SIMPLEX, AUTOSOMAL RECESSIVE 2
A
0.700
CausalMutation
CLINVAR
Founder mutation in dystonin-e underlying autosomal recessive epidermolysis bullosa simplex in Kuwait.
25059916
2015
rs185968827
DST;DST-AS1
Alzheimer's Disease
A
0.700
GeneticVariation
GWASCAT
Family-based association analyses of imputed genotypes reveal genome-wide significant association of Alzheimer's disease with OSBPL6, PTPRG, and PDCL3.
26830138
2016
rs950530102
×
Entrez Id:
667
Gene Symbol:
DST
DST
Bullous pemphigoid
0.010
GeneticVariation
BEFREE
Neither allelic nor genotypic BDNF Val66Met SNP was associated with dementia or with BP (associated or not with clinical manifestation of dementia).
30220011
2018
rs950530102
×
Entrez Id:
667
Gene Symbol:
DST
DST
Presenile dementia
0.010
GeneticVariation
BEFREE
Neither allelic nor genotypic BDNF Val66Met SNP was associated with dementia or with BP (associated or not with clinical manifestation of dementia ).
30220011
2018
rs950530102
×
Entrez Id:
667
Gene Symbol:
DST
DST
Dementia
0.010
GeneticVariation
BEFREE
Neither allelic nor genotypic BDNF Val66Met SNP was associated with dementia or with BP (associated or not with clinical manifestation of dementia ).
30220011
2018
rs2894837
×
Entrez Id:
667
Gene Symbol:
DST
DST
Forced expiratory volume function
A
0.700
GeneticVariation
GWASCAT
New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries.
30804560
2019