Disease: Sjogren-Larsson Syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs67939114
rs67939114
Entrez Id: 224
Gene Symbol: ALDH3A2
ALDH3A2
CUI: C0037231
Disease:
Sjogren-Larsson Syndrome 		0.700 GeneticVariation UNIPROT A novel point mutation of the FALDH gene in a Japanese family with Sjögren-Larsson syndrome. 10792573 2000
dbSNP: rs67939114
rs67939114
Entrez Id: 224
Gene Symbol: ALDH3A2
ALDH3A2
CUI: C0037231
Disease:
Sjogren-Larsson Syndrome 		0.700 GeneticVariation UNIPROT The molecular basis of Sjögren-Larsson syndrome: mutation analysis of the fatty aldehyde dehydrogenase gene. 10577908 1999
dbSNP: rs67939114
rs67939114
Entrez Id: 224
Gene Symbol: ALDH3A2
ALDH3A2
CUI: C0037231
Disease:
Sjogren-Larsson Syndrome 		0.700 GeneticVariation UNIPROT Spectrum of mutations and sequence variants in the FALDH gene in patients with Sjögren-Larsson syndrome. 9829906 1998
dbSNP: rs67939114
rs67939114
Entrez Id: 224
Gene Symbol: ALDH3A2
ALDH3A2
CUI: C0037231
Disease:
Sjogren-Larsson Syndrome 		0.700 GeneticVariation UNIPROT A missense mutation in the FALDH gene identified in Sjögren-Larsson syndrome patients originating from the northern part of Sweden. 9254849 1997
dbSNP: rs67939114
rs67939114
Entrez Id: 224
Gene Symbol: ALDH3A2
ALDH3A2
CUI: C0037231
Disease:
Sjogren-Larsson Syndrome 		0.700 GeneticVariation UNIPROT Sjögren-Larsson syndrome is caused by mutations in the fatty aldehyde dehydrogenase gene. 8528251 1996