Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs9635759
rs9635759
17 51536424 regulatory region variant G/A snv 0.25
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 5 2010 2019
dbSNP: rs7759938
rs7759938
0.925 0.120 6 104931079 intron variant C/T snv 0.62
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 4 2009 2018
dbSNP: rs3743266
rs3743266
15 60489314 3 prime UTR variant T/C snv 0.31
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 3 2010 2019
dbSNP: rs10423674
rs10423674
19 18707093 intron variant C/A;T snv
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 2 2010 2014
dbSNP: rs10453225
rs10453225
9 106157939 intron variant G/T snv 0.36
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 2 2009 2018
dbSNP: rs1079866
rs1079866
0.925 0.080 7 41430495 intergenic variant C/G snv 0.13
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 2 2010 2014
dbSNP: rs10938397
rs10938397
0.851 0.200 4 45180510 intergenic variant A/G snv 0.37
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 2 2010 2019
dbSNP: rs12472911
rs12472911
2 141470940 intron variant C/A;T snv
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 2 2010 2014
dbSNP: rs1364063
rs1364063
16 69554669 TF binding site variant T/C snv 0.35
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 2 2010 2014
dbSNP: rs1862471
rs1862471
19 9889646 intron variant C/G snv 0.38
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 2 2010 2016
dbSNP: rs2002675
rs2002675
3 185911780 downstream gene variant A/G snv 0.36
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 2 2010 2016
dbSNP: rs2090409
rs2090409
1.000 0.040 9 106204807 intron variant C/A;T snv
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 2 2009 2010
dbSNP: rs2687729
rs2687729
3 128176383 intron variant A/G snv 0.30
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 2 2010 2014
dbSNP: rs2947411
rs2947411
2 614168 intergenic variant A/G;T snv
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 2 2010 2014
dbSNP: rs466639
rs466639
1 165425645 intron variant T/A;C snv
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 2 2010 2014
dbSNP: rs4840086
rs4840086
6 99760562 intergenic variant A/G snv 0.33
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 2 2010 2014
dbSNP: rs6438424
rs6438424
3 117855975 intron variant A/C;T snv
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 2 2010 2016
dbSNP: rs6439371
rs6439371
3 132891908 intergenic variant G/A snv 0.63
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 2 2010 2019
dbSNP: rs6762477
rs6762477
3 50055776 intron variant G/A snv 0.64
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 2 2010 2014
dbSNP: rs7642134
rs7642134
3 86867732 intergenic variant A/G snv 0.55
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 2 2010 2014
dbSNP: rs7821178
rs7821178
0.925 0.080 8 77181601 intergenic variant C/A;G;T snv
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 2 2010 2014
dbSNP: rs852069
rs852069
20 17141948 intergenic variant A/G snv 0.57
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 2 2010 2014
dbSNP: rs900145
rs900145
11 13272358 upstream gene variant C/T snv 0.62
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 2 2010 2016
dbSNP: rs10441737
rs10441737
9 111539305 intron variant C/T snv 0.59
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 1 2013 2013
dbSNP: rs10899489
rs10899489
11 78384327 non coding transcript exon variant C/A;T snv
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 1 2010 2010