SCMH1, Scm polycomb group protein homolog 1, 22955

N. diseases: 11; N. variants: 11
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1032728
rs1032728
Entrez Id: 22955
Gene Symbol: SCMH1
SCMH1
CUI: C1314691
Disease:
Age at menarche
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1140227
rs1140227
Entrez Id: 22955;100507178
Gene Symbol: SCMH1;SLFNL1-AS1
SCMH1;SLFNL1-AS1
CUI: C0021704
Disease:
Intelligence
T 0.700 GeneticVariation GWASCAT A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence. 29326435 2019
dbSNP: rs114233776
rs114233776
Entrez Id: 22955
Gene Symbol: SCMH1
SCMH1
CUI: C0005890
Disease:
Body Height
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2749418
rs2749418
Entrez Id: 22955;100507178
Gene Symbol: SCMH1;SLFNL1-AS1
SCMH1;SLFNL1-AS1
CUI: C0042834
Disease:
Vital capacity
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2885697
rs2885697
Entrez Id: 22955
Gene Symbol: SCMH1
SCMH1
CUI: C0424678
Disease:
Lean body mass
0.700 GeneticVariation GWASCAT Genomics of body fat percentage may contribute to sex bias in anorexia nervosa. 30593698 2019
dbSNP: rs12024115
rs12024115
Entrez Id: 22955
Gene Symbol: SCMH1
SCMH1
CUI: C0596887
Disease:
mathematical ability
T 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs12024115
rs12024115
Entrez Id: 22955
Gene Symbol: SCMH1
SCMH1
CUI: C0596887
Disease:
mathematical ability
C 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs2284801
rs2284801
Entrez Id: 22955
Gene Symbol: SCMH1
SCMH1
CUI: C0596887
Disease:
mathematical ability
G 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs2885697
rs2885697
Entrez Id: 22955
Gene Symbol: SCMH1
SCMH1
CUI: C0004238
Disease:
Atrial Fibrillation
G 0.700 GeneticVariation GWASCAT Multi-ethnic genome-wide association study for atrial fibrillation. 29892015 2018
dbSNP: rs2885697
rs2885697
Entrez Id: 22955
Gene Symbol: SCMH1
SCMH1
CUI: C0004238
Disease:
Atrial Fibrillation
G 0.700 GeneticVariation GWASCAT Biobank-driven genomic discovery yields new insight into atrial fibrillation biology. 30061737 2018
dbSNP: rs35613919
rs35613919
Entrez Id: 22955
Gene Symbol: SCMH1
SCMH1
CUI: C0021704
Disease:
Intelligence
0.700 GeneticVariation GWASCAT Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. 29844566 2018
dbSNP: rs6600365
rs6600365
Entrez Id: 22955
Gene Symbol: SCMH1
SCMH1
CUI: C0005890
Disease:
Body Height
T 0.700 GeneticVariation GWASCAT Defining the role of common variation in the genomic and biological architecture of adult human height. 25282103 2014
dbSNP: rs11209718
rs11209718
Entrez Id: 22955
Gene Symbol: SCMH1
SCMH1
CUI: C0005890
Disease:
Body Height
T 0.700 GeneticVariation GWASCAT Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture. 23563607 2013
dbSNP: rs11209718
rs11209718
Entrez Id: 22955
Gene Symbol: SCMH1
SCMH1
CUI: C0489786
Disease:
Height
T 0.700 GeneticVariation GWASDB Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture. 23563607 2013
dbSNP: rs6686842
rs6686842
Entrez Id: 22955
Gene Symbol: SCMH1
SCMH1
CUI: C0005890
Disease:
Body Height
C 0.700 GeneticVariation GWASCAT Genome-wide association analysis identifies 20 loci that influence adult height. 18391952 2008
dbSNP: rs6686842
rs6686842
Entrez Id: 22955
Gene Symbol: SCMH1
SCMH1
CUI: C0489786
Disease:
Height
C 0.700 GeneticVariation GWASDB Genome-wide association analysis identifies 20 loci that influence adult height. 18391952 2008