Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121912296
rs121912296
Entrez Id: 1736
Gene Symbol: DKC1
DKC1
CUI: C1148551
Disease:
X-Linked Dyskeratosis Congenita
0.700 GeneticVariation UNIPROT Transcriptome-wide mapping reveals widespread dynamic-regulated pseudouridylation of ncRNA and mRNA. 25219674 2014
dbSNP: rs121912296
rs121912296
Entrez Id: 1736
Gene Symbol: DKC1
DKC1
CUI: C1148551
Disease:
X-Linked Dyskeratosis Congenita
0.700 GeneticVariation UNIPROT Telomere shortening and loss of self-renewal in dyskeratosis congenita induced pluripotent stem cells. 21602826 2011
dbSNP: rs121912296
rs121912296
Entrez Id: 1736
Gene Symbol: DKC1
DKC1
CUI: C1148551
Disease:
X-Linked Dyskeratosis Congenita
0.700 GeneticVariation UNIPROT Clinical utility gene card for: dyskeratosis congenita. 21610750 2011
dbSNP: rs121912296
rs121912296
Entrez Id: 1736
Gene Symbol: DKC1
DKC1
CUI: C1148551
Disease:
X-Linked Dyskeratosis Congenita
0.700 GeneticVariation UNIPROT Novel mutations of the DKC1 gene in individuals affected with dyskeratosis congenita. 19879169 2010
dbSNP: rs121912296
rs121912296
Entrez Id: 1736
Gene Symbol: DKC1
DKC1
CUI: C1148551
Disease:
X-Linked Dyskeratosis Congenita
0.700 GeneticVariation UNIPROT Pathogenic NAP57 mutations decrease ribonucleoprotein assembly in dyskeratosis congenita. 19734544 2009
dbSNP: rs121912296
rs121912296
Entrez Id: 1736
Gene Symbol: DKC1
DKC1
CUI: C1148551
Disease:
X-Linked Dyskeratosis Congenita
0.700 GeneticVariation UNIPROT Identification of a novel mutation in DKC1 in dyskeratosis congenita. 18802941 2009
dbSNP: rs121912296
rs121912296
Entrez Id: 1736
Gene Symbol: DKC1
DKC1
CUI: C1148551
Disease:
X-Linked Dyskeratosis Congenita
0.700 GeneticVariation UNIPROT X-linked dyskeratosis congenita in Malaysia. 17417794 2008
dbSNP: rs121912296
rs121912296
Entrez Id: 1736
Gene Symbol: DKC1
DKC1
CUI: C1148551
Disease:
X-Linked Dyskeratosis Congenita
0.700 GeneticVariation UNIPROT Identification of a novel mutation and a de novo mutation in DKC1 in two Chinese pedigrees with Dyskeratosis congenita. 15304085 2004
dbSNP: rs121912296
rs121912296
Entrez Id: 1736
Gene Symbol: DKC1
DKC1
CUI: C1148551
Disease:
X-Linked Dyskeratosis Congenita
0.700 GeneticVariation UNIPROT X-linked dyskeratosis congenita is predominantly caused by missense mutations in the DKC1 gene. 10364516 1999
dbSNP: rs121912296
rs121912296
Entrez Id: 1736
Gene Symbol: DKC1
DKC1
CUI: C1148551
Disease:
X-Linked Dyskeratosis Congenita
0.700 GeneticVariation UNIPROT X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functions. 9590285 1998