Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121908501
rs121908501
Entrez Id: 6777
Gene Symbol: STAT5B
STAT5B
CUI: C1855548
Disease:
Laron syndrome type 2
G 0.800 CausalMutation CLINVAR
dbSNP: rs121908502
rs121908502
Entrez Id: 6777
Gene Symbol: STAT5B
STAT5B
CUI: C1855548
Disease:
Laron syndrome type 2
A 0.700 CausalMutation CLINVAR
dbSNP: rs1555548678
rs1555548678
Entrez Id: 6777
Gene Symbol: STAT5B
STAT5B
CUI: C4072897
Disease:
Decreased serum insulin-like growth factor 1
A 0.700 CausalMutation CLINVAR
dbSNP: rs1555548678
rs1555548678
Entrez Id: 6777
Gene Symbol: STAT5B
STAT5B
CUI: C0349588
Disease:
Short stature
A 0.700 CausalMutation CLINVAR
dbSNP: rs1555548678
rs1555548678
Entrez Id: 6777
Gene Symbol: STAT5B
STAT5B
CUI: C1855548
Disease:
Laron syndrome type 2
A 0.700 CausalMutation CLINVAR
dbSNP: rs1555548678
rs1555548678
Entrez Id: 6777
Gene Symbol: STAT5B
STAT5B
CUI: C0878660
Disease:
Proportionate short stature
A 0.700 CausalMutation CLINVAR
dbSNP: rs1555548678
rs1555548678
Entrez Id: 6777
Gene Symbol: STAT5B
STAT5B
CUI: C3150077
Disease:
Mild short stature
A 0.700 CausalMutation CLINVAR
dbSNP: rs1555548678
rs1555548678
Entrez Id: 6777
Gene Symbol: STAT5B
STAT5B
CUI: C0236175
Disease:
Increased IgE level
A 0.700 CausalMutation CLINVAR
dbSNP: rs1555548678
rs1555548678
Entrez Id: 6777
Gene Symbol: STAT5B
STAT5B
CUI: C0013595
Disease:
Eczema
A 0.700 CausalMutation CLINVAR
dbSNP: rs1555548680
rs1555548680
Entrez Id: 6777
Gene Symbol: STAT5B
STAT5B
CUI: C0349588
Disease:
Short stature
C 0.700 CausalMutation CLINVAR
dbSNP: rs1555548680
rs1555548680
Entrez Id: 6777
Gene Symbol: STAT5B
STAT5B
CUI: C4072897
Disease:
Decreased serum insulin-like growth factor 1
C 0.700 CausalMutation CLINVAR
dbSNP: rs1555548680
rs1555548680
Entrez Id: 6777
Gene Symbol: STAT5B
STAT5B
CUI: C0878660
Disease:
Proportionate short stature
C 0.700 CausalMutation CLINVAR
dbSNP: rs1555548680
rs1555548680
Entrez Id: 6777
Gene Symbol: STAT5B
STAT5B
CUI: C1855548
Disease:
Laron syndrome type 2
C 0.700 CausalMutation CLINVAR
dbSNP: rs1555548680
rs1555548680
Entrez Id: 6777
Gene Symbol: STAT5B
STAT5B
CUI: C0236175
Disease:
Increased IgE level
C 0.700 CausalMutation CLINVAR
dbSNP: rs1555549674
rs1555549674
Entrez Id: 6777
Gene Symbol: STAT5B
STAT5B
CUI: C1855548
Disease:
Laron syndrome type 2
G 0.700 CausalMutation CLINVAR
dbSNP: rs1555549674
rs1555549674
Entrez Id: 6777
Gene Symbol: STAT5B
STAT5B
CUI: C4072897
Disease:
Decreased serum insulin-like growth factor 1
G 0.700 CausalMutation CLINVAR
dbSNP: rs1555549674
rs1555549674
Entrez Id: 6777
Gene Symbol: STAT5B
STAT5B
CUI: C0004096
Disease:
Asthma
G 0.700 CausalMutation CLINVAR
dbSNP: rs1555549674
rs1555549674
Entrez Id: 6777
Gene Symbol: STAT5B
STAT5B
CUI: C0878660
Disease:
Proportionate short stature
G 0.700 CausalMutation CLINVAR
dbSNP: rs1555549674
rs1555549674
Entrez Id: 6777
Gene Symbol: STAT5B
STAT5B
CUI: C0236175
Disease:
Increased IgE level
G 0.700 CausalMutation CLINVAR
dbSNP: rs1555549674
rs1555549674
Entrez Id: 6777
Gene Symbol: STAT5B
STAT5B
CUI: C0013595
Disease:
Eczema
G 0.700 CausalMutation CLINVAR
dbSNP: rs121908501
rs121908501
Entrez Id: 6777
Gene Symbol: STAT5B
STAT5B
CUI: C1855548
Disease:
Laron syndrome type 2
0.800 GeneticVariation UNIPROT Growth hormone insensitivity associated with a STAT5b mutation. 13679528 2003
dbSNP: rs121908501
rs121908501
Entrez Id: 6777
Gene Symbol: STAT5B
STAT5B
CUI: C1855548
Disease:
Laron syndrome type 2
0.800 GeneticVariation UNIPROT Severe growth hormone insensitivity resulting from total absence of signal transducer and activator of transcription 5b. 15827093 2005
dbSNP: rs761761205
rs761761205
Entrez Id: 6777
Gene Symbol: STAT5B
STAT5B
CUI: C1855548
Disease:
Laron syndrome type 2
TG 0.700 CausalMutation CLINVAR Clinical and biochemical characteristics of a male patient with a novel homozygous STAT5b mutation. 16787985 2006
dbSNP: rs6503691
rs6503691
Entrez Id: 6777
Gene Symbol: STAT5B
STAT5B
CUI: C0678222
Disease:
Breast Carcinoma
0.020 GeneticVariation BEFREE According to Akaike's information criterion, the best model to describe the relationship between the haplotypes and BC was based on the SNPs rs6503691 (STAT5B) and rs7211777 (STAT3). 17639043 2007
dbSNP: rs6503691
rs6503691
Entrez Id: 6777
Gene Symbol: STAT5B
STAT5B
CUI: C0006142
Disease:
Malignant neoplasm of breast
0.020 GeneticVariation BEFREE According to Akaike's information criterion, the best model to describe the relationship between the haplotypes and BC was based on the SNPs rs6503691 (STAT5B) and rs7211777 (STAT3). 17639043 2007