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: rs1041983
rs1041983
15 0.732 0.240 8 18400285 synonymous variant C/T snv 0.34 0.36 0.010 1.000 1 2009 2009
dbSNP: rs16906252
rs16906252
19 0.732 0.200 10 129467281 synonymous variant C/T snv 5.5E-02 5.1E-02 0.010 1.000 1 2011 2011
dbSNP: rs12947788
rs12947788
8 0.776 0.280 17 7674109 intron variant G/A snv 0.10 0.010 1.000 1 2013 2013
dbSNP: rs12951053
rs12951053
14 0.732 0.160 17 7674089 intron variant A/C snv 0.10 0.010 1.000 1 2013 2013
dbSNP: rs1508805
rs1508805
1 1.000 0.080 5 121634753 intergenic variant A/G snv 0.66 0.010 1.000 1 2015 2015
dbSNP: rs2501618
rs2501618
2 1.000 0.080 1 179989674 intron variant T/C snv 0.81 0.010 1.000 1 2015 2015
dbSNP: rs5756444
rs5756444
1 1.000 0.080 22 36982410 regulatory region variant T/C snv 0.34 0.010 1.000 1 2015 2015
dbSNP: rs28934574
rs28934574
31 0.658 0.440 17 7673776 missense variant G/A;C snv 4.0E-06 0.010 < 0.001 1 2016 2016
dbSNP: rs2235503
rs2235503
1 1.000 0.080 16 760593 upstream gene variant C/A snv 0.35 0.010 1.000 1 2017 2017
dbSNP: rs2235504
rs2235504
1 1.000 0.080 16 760655 upstream gene variant A/G snv 0.47 0.010 1.000 1 2017 2017
dbSNP: rs3764246
rs3764246
1 1.000 0.080 16 760143 upstream gene variant A/G snv 0.46 0.010 1.000 1 2017 2017
dbSNP: rs3764247
rs3764247
1 1.000 0.080 16 760039 upstream gene variant A/C snv 0.24 0.010 1.000 1 2017 2017
dbSNP: rs12150220
rs12150220
14 0.724 0.360 17 5582047 missense variant A/T snv 0.37 0.33 0.010 1.000 1 2018 2018
dbSNP: rs243865
rs243865
48 0.600 0.640 16 55477894 intron variant C/T snv 0.19 0.010 1.000 1 2018 2018
dbSNP: rs9939609
rs9939609
FTO
98 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2018 2018