Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12206564
rs12206564
Entrez Id: 10973
Gene Symbol: ASCC3
ASCC3
CUI: C1314691
Disease:
Age at menarche 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs12209887
rs12209887
Entrez Id: 10973
Gene Symbol: ASCC3
ASCC3
CUI: C1305855
Disease:
Body mass index 		A 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry. 30239722 2019
dbSNP: rs180963
rs180963
Entrez Id: 10973
Gene Symbol: ASCC3
ASCC3
CUI: C1305855
Disease:
Body mass index 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs239245
rs239245
Entrez Id: 10973
Gene Symbol: ASCC3
ASCC3
CUI: C0037369
Disease:
Smoking 		A 0.700 GeneticVariation GWASCAT Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences. 30643258 2019
dbSNP: rs6907240
rs6907240
Entrez Id: 10973
Gene Symbol: ASCC3
ASCC3
CUI: C1305855
Disease:
Body mass index 		T 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry. 30239722 2019
dbSNP: rs239198
rs239198
Entrez Id: 10973
Gene Symbol: ASCC3
ASCC3
CUI: C1314691
Disease:
Age at menarche 		T 0.700 GeneticVariation GWASCAT Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche. 25231870 2014
dbSNP: rs10485138
rs10485138
Entrez Id: 10973
Gene Symbol: ASCC3
ASCC3
CUI: C0019163
Disease:
Hepatitis B 		0.010 GeneticVariation BEFREE Our results indicated that SNP rs10485138 located in ASCC3 gene was associated with persistent HBV infection in Han Chinese. 26536629 2015