Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs17276588
rs17276588
Entrez Id: 10075;406889;407054
Gene Symbol: HUWE1;MIRLET7F2;MIR98
HUWE1;MIRLET7F2;MIR98
CUI: C0524620
Disease:
Metabolic Syndrome X
0.010 GeneticVariation BEFREE Additionally, interactions between rs7045890 and rs712, rs17276588 and rs10877887 were significantly associated with risk of MetS. 26178671 2015
dbSNP: rs17276588
rs17276588
Entrez Id: 10075;406889;407054
Gene Symbol: HUWE1;MIRLET7F2;MIR98
HUWE1;MIRLET7F2;MIR98
CUI: C0009402
Disease:
Colorectal Carcinoma
0.010 GeneticVariation BEFREE The rs17276588 AG and AG/AA genotypes had a significantly increased CRC</span> risk (AG vs. GG: adjusted odds ratio [OR] = 1.48, 95% confidence interval [CI] = 1.19-1.83, p < 0.001; AG/AA vs. GG: adjusted OR = 1.43, 95% CI = 1.17-1.75, p < 0.001). 30740676 2019
dbSNP: rs17276588
rs17276588
Entrez Id: 10075;406889;407054
Gene Symbol: HUWE1;MIRLET7F2;MIR98
HUWE1;MIRLET7F2;MIR98
CUI: C0017154
Disease:
Gastritis, Atrophic
0.010 GeneticVariation BEFREE A two-stage case-control study was designed to screen four miRNA SNPs (pri-let-7a-2 rs629367 and rs1143770, pri-let-7a-1 rs10739971, pri-let-7f-2 rs17276588) in 107 GC patients, 107 atrophic gastritis (AG), and matched 124 controls using PCR-RFLP. 24760009 2014
dbSNP: rs17276588
rs17276588
Entrez Id: 10075;406889;407054
Gene Symbol: HUWE1;MIRLET7F2;MIR98
HUWE1;MIRLET7F2;MIR98
CUI: C0027651
Disease:
Neoplasms
0.010 GeneticVariation BEFREE These findings indicate that the rs17276588 AG/AA genotypes increased CRC risk by reducing the expression of tumor suppressor let-7f. 30740676 2019
dbSNP: rs1057520538
rs1057520538
Entrez Id: 10075
Gene Symbol: HUWE1
HUWE1
CUI: C2678046
Disease:
Mental Retardation, X-Linked, Syndromic, Turner Type
A 0.700 CausalMutation CLINVAR
dbSNP: rs121918525
rs121918525
Entrez Id: 10075
Gene Symbol: HUWE1
HUWE1
CUI: C2678046
Disease:
Mental Retardation, X-Linked, Syndromic, Turner Type
A 0.700 CausalMutation CLINVAR
dbSNP: rs121918527
rs121918527
Entrez Id: 10075
Gene Symbol: HUWE1
HUWE1
CUI: C2678046
Disease:
Mental Retardation, X-Linked, Syndromic, Turner Type
A 0.700 CausalMutation CLINVAR
dbSNP: rs1556913268
rs1556913268
Entrez Id: 10075
Gene Symbol: HUWE1
HUWE1
CUI: C1854882
Disease:
Absent speech
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1556913268
rs1556913268
Entrez Id: 10075
Gene Symbol: HUWE1
HUWE1
CUI: C2678046
Disease:
Mental Retardation, X-Linked, Syndromic, Turner Type
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1556913268
rs1556913268
Entrez Id: 10075
Gene Symbol: HUWE1
HUWE1
CUI: C0333068
Disease:
Flexion contracture
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1556913268
rs1556913268
Entrez Id: 10075
Gene Symbol: HUWE1
HUWE1
CUI: C0423224
Disease:
Sunken eyes
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1556913268
rs1556913268
Entrez Id: 10075
Gene Symbol: HUWE1
HUWE1
CUI: C0036439
Disease:
Scoliosis, unspecified
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1556913268
rs1556913268
Entrez Id: 10075
Gene Symbol: HUWE1
HUWE1
CUI: C0036857
Disease:
Severe intellectual disability
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1556914274
rs1556914274
Entrez Id: 10075
Gene Symbol: HUWE1
HUWE1
CUI: C0423224
Disease:
Sunken eyes
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1556914274
rs1556914274
Entrez Id: 10075
Gene Symbol: HUWE1
HUWE1
CUI: C2315100
Disease:
Pediatric failure to thrive
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1556914274
rs1556914274
Entrez Id: 10075
Gene Symbol: HUWE1
HUWE1
CUI: C1854882
Disease:
Absent speech
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1556914274
rs1556914274
Entrez Id: 10075
Gene Symbol: HUWE1
HUWE1
CUI: C0011168
Disease:
Deglutition Disorders
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1556914274
rs1556914274
Entrez Id: 10075
Gene Symbol: HUWE1
HUWE1
CUI: C1837218
Disease:
Cleft palate, isolated
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1556914274
rs1556914274
Entrez Id: 10075
Gene Symbol: HUWE1
HUWE1
CUI: C0744356
Disease:
Abnormality of the genital system
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1556914274
rs1556914274
Entrez Id: 10075
Gene Symbol: HUWE1
HUWE1
CUI: C2678046
Disease:
Mental Retardation, X-Linked, Syndromic, Turner Type
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1556914274
rs1556914274
Entrez Id: 10075
Gene Symbol: HUWE1
HUWE1
CUI: C0042580
Disease:
Vesico-Ureteral Reflux
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1556914274
rs1556914274
Entrez Id: 10075
Gene Symbol: HUWE1
HUWE1
CUI: C1843367
Disease:
Poor school performance
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1556914274
rs1556914274
Entrez Id: 10075
Gene Symbol: HUWE1
HUWE1
CUI: C0005744
Disease:
Blepharophimosis
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1556914274
rs1556914274
Entrez Id: 10075
Gene Symbol: HUWE1
HUWE1
CUI: C0036857
Disease:
Severe intellectual disability
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1556914274
rs1556914274
Entrez Id: 10075
Gene Symbol: HUWE1
HUWE1
CUI: C3161330
Disease:
Profound intellectual disabilities
A 0.700 GeneticVariation CLINVAR