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: rs314268
rs314268
6 104970103 intron variant G/A snv 0.64
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.700 1.000 2 2009 2009
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: rs10156597
rs10156597
9 106179228 intron variant A/T snv 0.36
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.700 1.000 1 2009 2009
dbSNP: rs12352703
rs12352703
9 106154985 intron variant G/T snv 0.32
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.700 1.000 1 2009 2009
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: 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: 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: 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: 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: 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
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: rs314262
rs314262
6 104946746 intron variant G/A snv 0.46
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.700 1.000 1 2009 2009
dbSNP: rs314263
rs314263
6 104944870 intron variant C/T snv 0.69
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.700 1.000 1 2009 2009
dbSNP: rs314273
rs314273
6 105014007 intron variant T/G snv 0.64
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.700 1.000 1 2009 2009
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: rs369065
rs369065
6 104996183 intron variant C/T snv 0.63
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.700 1.000 1 2009 2009
dbSNP: rs395962
rs395962
6 104949543 intron variant T/G snv 0.72
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.700 1.000 1 2009 2009
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: rs7861820
rs7861820
9 106174393 intron variant T/C snv 0.62
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 1 2009 2009
dbSNP: rs9299121
rs9299121
9 106150131 intron variant T/A snv 0.32
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.700 1.000 1 2009 2009
dbSNP: rs9391253
rs9391253
6 104919741 intron variant A/T snv 0.29
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.700 1.000 1 2009 2009
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