SIM1, SIM bHLH transcription factor 1, 6492

N. diseases: 84; N. variants: 11
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1857859
rs1857859
Entrez Id: 6492
Gene Symbol: SIM1
SIM1
CUI: C0017654
Disease:
Glomerular Filtration Rate
A 0.700 GeneticVariation GWASCAT A catalog of genetic loci associated with kidney function from analyses of a million individuals. 31152163 2019
dbSNP: rs241812
rs241812
Entrez Id: 6492;102724406
Gene Symbol: SIM1;LOC102724406
SIM1;LOC102724406
CUI: C0201976
Disease:
Creatinine measurement, serum (procedure)
0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs241812
rs241812
Entrez Id: 6492;102724406
Gene Symbol: SIM1;LOC102724406
SIM1;LOC102724406
CUI: C0017654
Disease:
Glomerular Filtration Rate
0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs4840132
rs4840132
Entrez Id: 6492
Gene Symbol: SIM1
SIM1
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs3778033
rs3778033
Entrez Id: 6492;102724406
Gene Symbol: SIM1;LOC102724406
SIM1;LOC102724406
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs9386144
rs9386144
Entrez Id: 6492;102724406
Gene Symbol: SIM1;LOC102724406
SIM1;LOC102724406
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs3734354
rs3734354
Entrez Id: 6492;102724406
Gene Symbol: SIM1;LOC102724406
SIM1;LOC102724406
CUI: C0028754
Disease:
Obesity
0.020 GeneticVariation BEFREE Nevertheless, we found an association of rs3734354 in SIM1 with obesity of early-onset type in children, although not with obesity-related traits. 28593922 2017
dbSNP: rs3734354
rs3734354
Entrez Id: 6492;102724406
Gene Symbol: SIM1;LOC102724406
SIM1;LOC102724406
CUI: C0028754
Disease:
Obesity
0.020 GeneticVariation BEFREE Even though transmission disequilibrium test (TDT) further supported the association of P352T and +2,004 -/inst T with obesity, none of these nominal associations remained significant after a multiple testing Bonferroni correction. 20075856 2010
dbSNP: rs3734354
rs3734354
Entrez Id: 6492;102724406
Gene Symbol: SIM1;LOC102724406
SIM1;LOC102724406
CUI: C0023015
Disease:
Language Disorders
0.010 GeneticVariation BEFREE Firstly, we found a statistically significant association between the SIM1 SNP rs3734354 (Pro352Thr) and scores for language impairment (p = .0004), but due to low statistical power this should be interpreted cautiously. 24635660 2014
dbSNP: rs1004357606
rs1004357606
Entrez Id: 6492
Gene Symbol: SIM1
SIM1
CUI: C3809877
Disease:
Prader-Willi-like syndrome
0.010 GeneticVariation BEFREE We identified 4 rare variants (p.I128T, p.Q152E, p.R581G, and p.T714A) in 4 children with Prader-Willi-like syndrome features (including severe obesity) and 4 other rare variants (p.T46R, p.E62K, p.H323Y, and p.D740H) in 7 morbidly obese adults. 23778136 2013
dbSNP: rs201038781
rs201038781
Entrez Id: 6492
Gene Symbol: SIM1
SIM1
CUI: C3809877
Disease:
Prader-Willi-like syndrome
0.010 GeneticVariation BEFREE We identified 4 rare variants (p.I128T, p.Q152E, p.R581G, and p.T714A) in 4 children with Prader-Willi-like syndrome features (including severe obesity) and 4 other rare variants (p.T46R, p.E62K, p.H323Y, and p.D740H) in 7 morbidly obese adults. 23778136 2013
dbSNP: rs756633599
rs756633599
Entrez Id: 6492
Gene Symbol: SIM1
SIM1
CUI: C3809877
Disease:
Prader-Willi-like syndrome
0.010 GeneticVariation BEFREE We identified 4 rare variants (p.I128T, p.Q152E, p.R581G, and p.T714A) in 4 children with Prader-Willi-like syndrome features (including severe obesity) and 4 other rare variants (p.T46R, p.E62K, p.H323Y, and p.D740H) in 7 morbidly obese adults. 23778136 2013
dbSNP: rs756633599
rs756633599
Entrez Id: 6492
Gene Symbol: SIM1
SIM1
CUI: C0028754
Disease:
Obesity
0.010 GeneticVariation BEFREE Three mutations showed strong loss-of-function effects (p.T46R, p.H323Y, and p.T714A) and were associated with high intra-family risk for obesity, while the variants with mild or no effects on SIM1 activity were not associated with obesity within families. 23778136 2013
dbSNP: rs757139012
rs757139012
Entrez Id: 6492
Gene Symbol: SIM1
SIM1
CUI: C0028756
Disease:
Obesity, Morbid
0.010 GeneticVariation BEFREE We identified 4 rare variants (p.I128T, p.Q152E, p.R581G, and p.T714A) in 4 children with Prader-Willi-like syndrome features (including severe obesity) and 4 other rare variants (p.T46R, p.E62K, p.H323Y, and p.D740H) in 7 morbidly obese adults. 23778136 2013
dbSNP: rs757139012
rs757139012
Entrez Id: 6492
Gene Symbol: SIM1
SIM1
CUI: C3809877
Disease:
Prader-Willi-like syndrome
0.010 GeneticVariation BEFREE We identified 4 rare variants (p.I128T, p.Q152E, p.R581G, and p.T714A) in 4 children with Prader-Willi-like syndrome features (including severe obesity) and 4 other rare variants (p.T46R, p.E62K, p.H323Y, and p.D740H) in 7 morbidly obese adults. 23778136 2013
dbSNP: rs757139012
rs757139012
Entrez Id: 6492
Gene Symbol: SIM1
SIM1
CUI: C0028754
Disease:
Obesity
0.010 GeneticVariation BEFREE Three mutations showed strong loss-of-function effects (p.T46R, p.H323Y, and p.T714A) and were associated with high intra-family risk for obesity, while the variants with mild or no effects on SIM1 activity were not associated with obesity within families. 23778136 2013
dbSNP: rs3213541
rs3213541
Entrez Id: 6492
Gene Symbol: SIM1
SIM1
CUI: C0028754
Disease:
Obesity
0.010 GeneticVariation BEFREE Two variants (rs3734353 and rs3213541) were also genotyped in 1,275 severely obese and 1,395 lean control subjects of French European ancestry. 19401419 2009