Source: GWASCAT ×
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2916733
rs2916733
MCPH1
1 0.851 0.120 8 6465757 intron variant G/A snv 0.28 0.810 1.000 1 2011 2011
dbSNP: rs116855232
rs116855232
NUDT15
4 0.742 0.400 13 48045719 missense variant C/T snv 2.8E-02 1.1E-02 0.800 1.000 3 2014 2020
dbSNP: rs79206939
rs79206939
FTO
2 0.925 0.160 16 53826140 missense variant G/A snv 2.1E-03 6.4E-04 0.710 1.000 1 2017 2017
dbSNP: rs117506642
rs117506642
LOC105376755
2 1.000 0.040 2 195143585 intergenic variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs117829974
rs117829974 		2 1.000 0.040 3 62886233 intergenic variant C/A;G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs2501846
rs2501846 		2 1.000 0.040 1 212668592 upstream gene variant T/C snv 0.24 0.700 1.000 1 2018 2018