Source: GWASDB

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: rs1516881
rs1516881
9 106150773 intron variant C/G;T snv
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.700 1.000 1 2009 2009
dbSNP: rs1516882
rs1516882
9 106150630 intron variant A/G snv 0.32
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.700 1.000 1 2009 2009
dbSNP: rs1516883
rs1516883
9 106144986 intron variant G/A snv 0.32
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 1 2009 2018
dbSNP: rs1516890
rs1516890
9 106227118 intron variant G/A snv 0.56
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.700 1.000 1 2009 2009
dbSNP: rs1659127
rs1659127
16 14294448 intergenic variant G/A;C;T snv
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 1 2010 2010
dbSNP: rs167539
rs167539
6 104962173 intron variant C/A snv 0.64
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.700 1.000 1 2009 2009
dbSNP: rs16938437
rs16938437
11 46031024 intron variant C/T snv 0.13
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 1 2010 2010
dbSNP: rs17034020
rs17034020
4 103729516 intergenic variant G/A snv 9.8E-02
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.700 1.000 1 2010 2010
dbSNP: rs17034046
rs17034046
4 103738447 intergenic variant C/A;T snv
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.700 1.000 1 2010 2010
dbSNP: rs17188434
rs17188434
2 156240264 intron variant T/C snv 4.4E-02
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 1 2010 2010
dbSNP: rs17196160
rs17196160
4 103736685 intergenic variant T/C snv 4.6E-02
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.700 1.000 1 2010 2010
dbSNP: rs17196407
rs17196407
4 103742364 intergenic variant C/T snv 4.1E-02
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.700 1.000 1 2010 2010
dbSNP: rs17249293
rs17249293
4 103735627 intergenic variant G/A;T snv
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.700 1.000 1 2010 2010
dbSNP: rs17249363
rs17249363
4 103736532 intergenic variant A/G snv 4.6E-02
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.700 1.000 1 2010 2010
dbSNP: rs17268785
rs17268785
2 56364948 intron variant A/G snv 0.20
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 1 2010 2010
dbSNP: rs17669535
rs17669535
8 1295964 intron variant C/G snv 7.4E-02
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 1 2013 2013
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 1 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 1 2010 2016
dbSNP: rs2008393
rs2008393
9 106151776 intron variant A/G snv 0.32
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.700 1.000 1 2009 2009
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: rs2095812
rs2095812
6 104936103 non coding transcript exon variant C/G snv 0.31
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.700 1.000 1 2009 2009
dbSNP: rs2138628
rs2138628
9 106169451 intron variant T/A;C;G snv
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.700 1.000 1 2009 2009
dbSNP: rs2222133
rs2222133
9 106154791 intron variant T/C snv 0.33
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.700 1.000 1 2009 2009
dbSNP: rs2243803
rs2243803
18 45376707 intron variant T/A snv 0.53
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 1 2010 2010
dbSNP: rs2348186
rs2348186
5 137088070 intron variant T/C snv 0.40
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.700 1.000 1 2009 2009