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: 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: 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: rs10007754
rs10007754
4 103706285 intron variant T/G snv 0.34
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.700 1.000 1 2010 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: 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: rs10913469
rs10913469
1.000 0.080 1 177944384 intron variant T/C snv 0.22
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.700 1.000 1 2010 2010
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: rs12617311
rs12617311
2 198767841 intron variant G/A snv 0.28
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 1 2010 2010
dbSNP: rs13187289
rs13187289
5 134513486 upstream gene variant C/A;G snv 0.19
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 1 2010 2010
dbSNP: rs1361108
rs1361108
6 126446454 intron variant C/T snv 0.44
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 1 2010 2010
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: 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: 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: 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: 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: rs2815752
rs2815752
0.925 0.200 1 72346757 intron variant G/A snv 0.62
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.700 1.000 1 2010 2010