Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104893765
rs104893765
0.800 GeneticVariation UNIPROT Identification and functional analysis of the novel S179R POU1F1 mutation associated with combined pituitary hormone deficiency. 16968807

2006

dbSNP: rs104893766
rs104893766
0.800 GeneticVariation UNIPROT Identification and functional analysis of the novel S179R POU1F1 mutation associated with combined pituitary hormone deficiency. 16968807

2006

dbSNP: rs104893756
rs104893756
0.800 GeneticVariation UNIPROT Novel mutations within the POU1F1 gene associated with variable combined pituitary hormone deficiency. 15928241

2005

dbSNP: rs104893757
rs104893757
0.800 GeneticVariation UNIPROT Novel mutations within the POU1F1 gene associated with variable combined pituitary hormone deficiency. 15928241

2005

dbSNP: rs104893758
rs104893758
0.800 GeneticVariation UNIPROT Novel mutations within the POU1F1 gene associated with variable combined pituitary hormone deficiency. 15928241

2005

dbSNP: rs104893759
rs104893759
0.800 GeneticVariation UNIPROT Novel mutations within the POU1F1 gene associated with variable combined pituitary hormone deficiency. 15928241

2005

dbSNP: rs104893761
rs104893761
0.800 GeneticVariation UNIPROT Novel mutations within the POU1F1 gene associated with variable combined pituitary hormone deficiency. 15928241

2005

dbSNP: rs104893762
rs104893762
0.800 GeneticVariation UNIPROT Novel mutations within the POU1F1 gene associated with variable combined pituitary hormone deficiency. 15928241

2005

dbSNP: rs104893764
rs104893764
0.800 GeneticVariation UNIPROT Novel mutations within the POU1F1 gene associated with variable combined pituitary hormone deficiency. 15928241

2005

dbSNP: rs104893765
rs104893765
0.800 GeneticVariation UNIPROT Novel mutations within the POU1F1 gene associated with variable combined pituitary hormone deficiency. 15928241

2005

dbSNP: rs104893766
rs104893766
0.800 GeneticVariation UNIPROT Novel mutations within the POU1F1 gene associated with variable combined pituitary hormone deficiency. 15928241

2005

dbSNP: rs104893756
rs104893756
0.800 GeneticVariation UNIPROT Combined pituitary hormone deficiency caused by compound heterozygosity for two novel mutations in the POU domain of the Pit1/POU1F1 gene. 11297581

2001

dbSNP: rs104893757
rs104893757
0.800 GeneticVariation UNIPROT Combined pituitary hormone deficiency caused by compound heterozygosity for two novel mutations in the POU domain of the Pit1/POU1F1 gene. 11297581

2001

dbSNP: rs104893758
rs104893758
0.800 GeneticVariation UNIPROT Combined pituitary hormone deficiency caused by compound heterozygosity for two novel mutations in the POU domain of the Pit1/POU1F1 gene. 11297581

2001

dbSNP: rs104893759
rs104893759
0.800 GeneticVariation UNIPROT Combined pituitary hormone deficiency caused by compound heterozygosity for two novel mutations in the POU domain of the Pit1/POU1F1 gene. 11297581

2001

dbSNP: rs104893761
rs104893761
0.800 GeneticVariation UNIPROT Combined pituitary hormone deficiency caused by compound heterozygosity for two novel mutations in the POU domain of the Pit1/POU1F1 gene. 11297581

2001

dbSNP: rs104893762
rs104893762
0.800 GeneticVariation UNIPROT Combined pituitary hormone deficiency caused by compound heterozygosity for two novel mutations in the POU domain of the Pit1/POU1F1 gene. 11297581

2001

dbSNP: rs104893764
rs104893764
0.800 GeneticVariation UNIPROT Combined pituitary hormone deficiency caused by compound heterozygosity for two novel mutations in the POU domain of the Pit1/POU1F1 gene. 11297581

2001

dbSNP: rs104893765
rs104893765
0.800 GeneticVariation UNIPROT Combined pituitary hormone deficiency caused by compound heterozygosity for two novel mutations in the POU domain of the Pit1/POU1F1 gene. 11297581

2001

dbSNP: rs104893766
rs104893766
0.800 GeneticVariation UNIPROT Combined pituitary hormone deficiency caused by compound heterozygosity for two novel mutations in the POU domain of the Pit1/POU1F1 gene. 11297581

2001

dbSNP: rs104893756
rs104893756
0.800 GeneticVariation UNIPROT Pro239Ser: a novel recessive mutation of the Pit-1 gene in seven Middle Eastern children with growth hormone, prolactin, and thyrotropin deficiency. 9626142

1998

dbSNP: rs104893756
rs104893756
0.800 GeneticVariation UNIPROT Central hypothyroidism reveals compound heterozygous mutations in the Pit-1 gene. 9485179

1998

dbSNP: rs104893757
rs104893757
0.800 GeneticVariation UNIPROT Pro239Ser: a novel recessive mutation of the Pit-1 gene in seven Middle Eastern children with growth hormone, prolactin, and thyrotropin deficiency. 9626142

1998

dbSNP: rs104893757
rs104893757
0.800 GeneticVariation UNIPROT Central hypothyroidism reveals compound heterozygous mutations in the Pit-1 gene. 9485179

1998

dbSNP: rs104893758
rs104893758
0.800 GeneticVariation UNIPROT Central hypothyroidism reveals compound heterozygous mutations in the Pit-1 gene. 9485179

1998