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: 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: 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: 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: rs10441737
rs10441737
9 111539305 intron variant C/T snv 0.59
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 1 2013 2013
dbSNP: rs10453225
rs10453225
9 106157939 intron variant G/T snv 0.36
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 1 2009 2018
dbSNP: rs1079866
rs1079866
0.925 0.080 7 41430495 intergenic variant C/G snv 0.13
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: 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: rs10940138
rs10940138
5 67898641 intron variant C/T snv 0.21
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 1 2013 2013
dbSNP: rs10978430
rs10978430
9 106153728 intron variant C/T snv 0.33
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 1 2009 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: 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: 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: rs12686569
rs12686569
9 106154430 intron variant G/T snv 0.30
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 1 2009 2016
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: 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: rs1351623
rs1351623
4 103666820 intron variant C/T snv 0.36
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 1 2010 2019
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: rs1364063
rs1364063
16 69554669 TF binding site variant T/C snv 0.35
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: 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: 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: 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