Source: GWASCAT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs100537
rs100537
RXRG
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.700 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965

2016
dbSNP: rs10060622
rs10060622
LINC00461
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
dbSNP: rs10063744
rs10063744
LOC101929710
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
dbSNP: rs10094574
rs10094574
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.700 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965

2016
dbSNP: rs10119582
rs10119582
PTPRD
CUI: C1314691
Disease: Age at menarche
Age at menarche 		C 0.700 GeneticVariation GWASCAT Elucidating the genetic architecture of reproductive ageing in the Japanese population. 29773799

2018
dbSNP: rs10136330
rs10136330
PRKD1
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
dbSNP: rs10144321
rs10144321
WDR25
CUI: C1314691
Disease: Age at menarche
Age at menarche 		A 0.700 GeneticVariation GWASCAT Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche. 25231870

2014
dbSNP: rs10150590
rs10150590
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
dbSNP: rs10170108
rs10170108
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
dbSNP: rs10217747
rs10217747
ZNF483
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.700 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965

2016
dbSNP: rs10226266
rs10226266
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
dbSNP: rs10232457
rs10232457
SLC25A40
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.700 GeneticVariation GWASCAT Bivariate Genome-Wide Association Study Implicates ATP6V1G1 as a Novel Pleiotropic Locus Underlying Osteoporosis and Age at Menarche. 26312577

2015
dbSNP: rs10264856
rs10264856
ABCB1 ; RUNDC3B
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.700 GeneticVariation GWASCAT Bivariate Genome-Wide Association Study Implicates ATP6V1G1 as a Novel Pleiotropic Locus Underlying Osteoporosis and Age at Menarche. 26312577

2015
dbSNP: rs1032728
rs1032728
SCMH1
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
dbSNP: rs1038903
rs1038903
CUI: C1314691
Disease: Age at menarche
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: rs1040070
rs1040070
TNNI3K ; FPGT-TNNI3K ; LRRC53
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.700 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965

2016
dbSNP: rs10401175
rs10401175
MAST3
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
dbSNP: rs10423674
rs10423674
CRTC1
CUI: C1314691
Disease: Age at menarche
Age at menarche 		A 0.800 GeneticVariation GWASCAT Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. 21102462

2010
dbSNP: rs10423674
rs10423674
CRTC1
CUI: C1314691
Disease: Age at menarche
Age at menarche 		A 0.800 GeneticVariation GWASCAT Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche. 25231870

2014
dbSNP: rs10441737
rs10441737
ZNF483
CUI: C1314691
Disease: Age at menarche
Age at menarche 		T 0.800 GeneticVariation GWASCAT Genome-wide association study of age at menarche in African-American women. 23599027

2013
dbSNP: rs10453225
rs10453225
LINC01505
CUI: C1314691
Disease: Age at menarche
Age at menarche 		G 0.800 GeneticVariation GWASCAT Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche. 25231870

2014
dbSNP: rs10453225
rs10453225
LINC01505
CUI: C1314691
Disease: Age at menarche
Age at menarche 		G 0.800 GeneticVariation GWASCAT Elucidating the genetic architecture of reproductive ageing in the Japanese population. 29773799

2018
dbSNP: rs1045590
rs1045590
RSF1
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
dbSNP: rs1054442
rs1054442
DDN
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
dbSNP: rs10739221
rs10739221
LINC01505
CUI: C1314691
Disease: Age at menarche
Age at menarche 		C 0.700 GeneticVariation GWASCAT Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche. 25231870

2014