Source: ALL

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: rs10453225
rs10453225
LINC01505
9 106157939 intron variant G/T snv 0.36
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.800 1.000 3 2009 2018
dbSNP: rs10978430
rs10978430
LINC01505
9 106153728 intron variant C/T snv 0.33
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.800 1.000 2 2009 2019
dbSNP: rs12686569
rs12686569
LINC01505
9 106154430 intron variant G/T snv 0.30
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.800 1.000 2 2009 2016
dbSNP: rs1516883
rs1516883
LINC01505
9 106144986 intron variant G/A snv 0.32
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.800 1.000 2 2009 2018
dbSNP: rs2090409
rs2090409
LINC01505
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: rs7861820
rs7861820
LINC01505
9 106174393 intron variant T/C snv 0.62
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.800 1.000 2 2009 2009
dbSNP: rs10156597
rs10156597
LINC01505
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: rs10739221
rs10739221
LINC01505
0.851 0.080 9 106298549 intron variant T/C;G snv
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.700 1.000 1 2014 2014
dbSNP: rs10816359
rs10816359
LINC01505
9 105995389 intron variant T/G snv 0.18
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.700 1.000 1 2014 2014
dbSNP: rs12352703
rs12352703
LINC01505
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
LINC01505
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
LINC01505
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
LINC01505
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: rs2008393
rs2008393
LINC01505
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: rs2138628
rs2138628
LINC01505
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
LINC01505
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: rs2417687
rs2417687
LINC01505
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: rs9299121
rs9299121
LINC01505
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: rs9409084
rs9409084
LINC01505
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: rs966523
rs966523
LINC01505
9 106295166 intron variant C/G;T snv
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.700 1.000 1 2009 2009