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: 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: 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: rs10019555
rs10019555
4 103694124 intron variant G/A;C snv
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.700 1.000 1 2010 2010
dbSNP: rs10423674
rs10423674
19 18707093 intron variant C/A;T snv
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 1 2010 2014
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
dbSNP: rs12472911
rs12472911
2 141470940 intron variant C/A;T snv
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 1 2010 2014
dbSNP: rs1398217
rs1398217
18 47225867 intron variant G/C;T snv
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 1 2010 2010
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: 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: 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: 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: 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: 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: 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
dbSNP: rs364663
rs364663
6 104995314 intron variant T/A;G snv
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 1 2013 2013
dbSNP: rs4549631
rs4549631
6 126645162 intron variant T/C;G snv
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.700 1.000 1 2010 2010
dbSNP: rs466639
rs466639
1 165425645 intron variant T/A;C snv
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 1 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 1 2010 2016
dbSNP: rs757647
rs757647
5 138371626 intron variant G/A;C snv
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 1 2010 2010
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 1 2010 2014
dbSNP: rs9555810
rs9555810
13 111529090 intergenic variant C/G;T snv
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 1 2010 2010
dbSNP: rs966523
rs966523
9 106295166 intron variant C/G;T snv
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.700 1.000 1 2009 2009
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: 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: 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