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: rs314276
rs314276
0.807 0.280 6 104960124 intron variant A/C snv 0.65
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 2 2009 2009
dbSNP: rs1482582
rs1482582
4 103730396 intergenic variant A/C snv 0.34
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.700 1.000 1 2010 2010
dbSNP: rs6589964
rs6589964
11 122999975 intergenic variant A/C snv 0.54
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 1 2010 2010
dbSNP: rs7617480
rs7617480
3 49173299 intron variant A/C snv 0.76
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 1 2010 2010
dbSNP: rs314277
rs314277
0.925 0.080 6 104959787 intron variant A/C;G;T snv
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 2 2009 2010
dbSNP: rs2417687
rs2417687
9 106161176 intron variant A/C;G;T snv
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.700 1.000 1 2009 2009
dbSNP: rs6438424
rs6438424
3 117855975 intron variant A/C;T snv
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 1 2010 2016
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 1 2010 2019
dbSNP: rs10980926
rs10980926
9 111531354 intron variant A/G snv 0.56
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 1 2010 2010
dbSNP: rs12907866
rs12907866
15 51253257 intron variant A/G snv 0.35
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 1 2013 2013
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: 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: 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: rs2687729
rs2687729
3 128176383 intron variant A/G snv 0.30
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 1 2010 2014
dbSNP: rs314280
rs314280
0.925 0.040 6 104952962 intron variant A/G snv 0.46
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 1 2009 2009
dbSNP: rs320320
rs320320
1 243671884 intron variant A/G snv 0.30
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 1 2013 2013
dbSNP: rs3733632
rs3733632
4 103719778 5 prime UTR variant A/G snv 0.34
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.700 1.000 1 2010 2010
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 1 2010 2014
dbSNP: rs4946651
rs4946651
6 104921635 intron variant A/G snv 0.46
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.700 1.000 1 2009 2009
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 1 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 1 2010 2014
dbSNP: rs9409084
rs9409084
9 106145365 intron variant A/G snv 0.51
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.700 1.000 1 2009 2009
dbSNP: rs2947411
rs2947411
2 614168 intergenic variant A/G;T snv
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 1 2010 2014