Gene: ANOS1 ×
Source: UNIPROT ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1170543613
rs1170543613
ANOS1
0.700 GeneticVariation UNIPROT

dbSNP: rs137900287
rs137900287
ANOS1
0.700 GeneticVariation UNIPROT

dbSNP: rs199771303
rs199771303
ANOS1
0.700 GeneticVariation UNIPROT

dbSNP: rs137852515
rs137852515
ANOS1
0.800 GeneticVariation UNIPROT Heterogeneity in the mutations responsible for X chromosome-linked Kallmann syndrome. 8504298

1993
dbSNP: rs137852517
rs137852517
ANOS1
0.800 GeneticVariation UNIPROT Heterogeneity in the mutations responsible for X chromosome-linked Kallmann syndrome. 8504298

1993
dbSNP: rs1394625082
rs1394625082
ANOS1
0.700 GeneticVariation UNIPROT Heterogeneity in the mutations responsible for X chromosome-linked Kallmann syndrome. 8504298

1993
dbSNP: rs140812865
rs140812865
ANOS1
0.700 GeneticVariation UNIPROT Heterogeneity in the mutations responsible for X chromosome-linked Kallmann syndrome. 8504298

1993
dbSNP: rs144586521
rs144586521
ANOS1
0.700 GeneticVariation UNIPROT Heterogeneity in the mutations responsible for X chromosome-linked Kallmann syndrome. 8504298

1993
dbSNP: rs137852515
rs137852515
ANOS1
0.800 GeneticVariation UNIPROT Genetic heterogeneity evidenced by low incidence of KAL-1 gene mutations in sporadic cases of gonadotropin-releasing hormone deficiency. 8989261

1997
dbSNP: rs137852517
rs137852517
ANOS1
0.800 GeneticVariation UNIPROT Genetic heterogeneity evidenced by low incidence of KAL-1 gene mutations in sporadic cases of gonadotropin-releasing hormone deficiency. 8989261

1997
dbSNP: rs1394625082
rs1394625082
ANOS1
0.700 GeneticVariation UNIPROT Genetic heterogeneity evidenced by low incidence of KAL-1 gene mutations in sporadic cases of gonadotropin-releasing hormone deficiency. 8989261

1997
dbSNP: rs140812865
rs140812865
ANOS1
0.700 GeneticVariation UNIPROT Genetic heterogeneity evidenced by low incidence of KAL-1 gene mutations in sporadic cases of gonadotropin-releasing hormone deficiency. 8989261

1997
dbSNP: rs144586521
rs144586521
ANOS1
0.700 GeneticVariation UNIPROT Genetic heterogeneity evidenced by low incidence of KAL-1 gene mutations in sporadic cases of gonadotropin-releasing hormone deficiency. 8989261

1997
dbSNP: rs137852515
rs137852515
ANOS1
0.800 GeneticVariation UNIPROT A recurrent missense mutation in the KAL gene in patients with X-linked Kallmann's syndrome. 9589672

1998
dbSNP: rs137852517
rs137852517
ANOS1
0.800 GeneticVariation UNIPROT A recurrent missense mutation in the KAL gene in patients with X-linked Kallmann's syndrome. 9589672

1998
dbSNP: rs1394625082
rs1394625082
ANOS1
0.700 GeneticVariation UNIPROT A recurrent missense mutation in the KAL gene in patients with X-linked Kallmann's syndrome. 9589672

1998
dbSNP: rs140812865
rs140812865
ANOS1
0.700 GeneticVariation UNIPROT A recurrent missense mutation in the KAL gene in patients with X-linked Kallmann's syndrome. 9589672

1998
dbSNP: rs144586521
rs144586521
ANOS1
0.700 GeneticVariation UNIPROT A recurrent missense mutation in the KAL gene in patients with X-linked Kallmann's syndrome. 9589672

1998
dbSNP: rs137852515
rs137852515
ANOS1
0.800 GeneticVariation UNIPROT The importance of autosomal genes in Kallmann syndrome: genotype-phenotype correlations and neuroendocrine characteristics. 11297579

2001
dbSNP: rs137852517
rs137852517
ANOS1
0.800 GeneticVariation UNIPROT The importance of autosomal genes in Kallmann syndrome: genotype-phenotype correlations and neuroendocrine characteristics. 11297579

2001
dbSNP: rs1394625082
rs1394625082
ANOS1
0.700 GeneticVariation UNIPROT The importance of autosomal genes in Kallmann syndrome: genotype-phenotype correlations and neuroendocrine characteristics. 11297579

2001
dbSNP: rs140812865
rs140812865
ANOS1
0.700 GeneticVariation UNIPROT The importance of autosomal genes in Kallmann syndrome: genotype-phenotype correlations and neuroendocrine characteristics. 11297579

2001
dbSNP: rs144586521
rs144586521
ANOS1
0.700 GeneticVariation UNIPROT The importance of autosomal genes in Kallmann syndrome: genotype-phenotype correlations and neuroendocrine characteristics. 11297579

2001
dbSNP: rs137852515
rs137852515
ANOS1
0.800 GeneticVariation UNIPROT Clinical assessment and mutation analysis of Kallmann syndrome 1 (KAL1) and fibroblast growth factor receptor 1 (FGFR1, or KAL2) in five families and 18 sporadic patients. 15001591

2004
dbSNP: rs137852517
rs137852517
ANOS1
0.800 GeneticVariation UNIPROT Clinical assessment and mutation analysis of Kallmann syndrome 1 (KAL1) and fibroblast growth factor receptor 1 (FGFR1, or KAL2) in five families and 18 sporadic patients. 15001591

2004