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: rs1473473
rs1473473
4 0.925 0.080 12 72010598 intron variant C/A;T snv 0.81 0.020 1.000 2 2011 2013
dbSNP: rs10096097
rs10096097
1 1.000 0.040 8 30169582 intron variant G/A snv 0.62 0.010 1.000 1 2011 2011
dbSNP: rs3749073
rs3749073
1 1.000 0.040 2 230910379 missense variant C/A snv 0.12 0.17 0.010 1.000 1 2011 2011
dbSNP: rs533123
rs533123
3 0.882 0.160 1 28814643 intron variant G/A;C snv 0.010 1.000 1 2011 2011
dbSNP: rs7532266
rs7532266
1 1.000 0.040 1 23225130 regulatory region variant A/C snv 0.66 0.010 1.000 1 2011 2011
dbSNP: rs774996029
rs774996029
1 1.000 0.040 20 62709682 missense variant G/A snv 4.0E-06 1.4E-05 0.010 1.000 1 2012 2012
dbSNP: rs9939609
rs9939609
FTO
98 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2012 2012
dbSNP: rs10070190
rs10070190
2 0.925 0.040 5 26866262 intergenic variant G/A snv 0.60 0.010 1.000 1 2013 2013
dbSNP: rs11179027
rs11179027
1 1.000 0.040 12 71983532 intron variant G/C snv 0.26 0.010 1.000 1 2013 2013
dbSNP: rs11783752
rs11783752
2 0.925 0.040 8 20192013 intergenic variant G/A;C snv 0.010 1.000 1 2013 2013
dbSNP: rs1285957
rs1285957
1 1.000 0.040 7 141889478 downstream gene variant T/C snv 0.86 0.700 1.000 1 2013 2013
dbSNP: rs145241704
rs145241704
1 1.000 0.040 7 141805287 upstream gene variant T/G snv 7.4E-02 0.800 1.000 1 2013 2013
dbSNP: rs2834070
rs2834070
2 0.925 0.040 21 33015144 intron variant G/T snv 0.24 0.010 1.000 1 2013 2013
dbSNP: rs3825885
rs3825885
1 1.000 0.040 15 88059610 intron variant T/C snv 0.32 0.010 1.000 1 2013 2013
dbSNP: rs4825476
rs4825476
2 0.925 0.040 X 123307628 intron variant G/A;C snv 0.010 1.000 1 2013 2013
dbSNP: rs56156506
rs56156506
1 1.000 0.040 X 38140399 intron variant A/T snv 0.33 0.800 1.000 1 2013 2013
dbSNP: rs62090893
rs62090893
1 1.000 0.040 18 75338379 intergenic variant G/A snv 9.7E-02 0.800 1.000 1 2013 2013
dbSNP: rs1042571
rs1042571
3 0.882 0.120 2 25161018 3 prime UTR variant G/A snv 0.16 0.010 1.000 1 2014 2014
dbSNP: rs13338499
rs13338499
2 0.925 0.040 16 67486220 intron variant A/G;T snv 0.010 1.000 1 2014 2014
dbSNP: rs3798577
rs3798577
16 0.742 0.320 6 152099995 3 prime UTR variant T/C snv 0.45 0.010 1.000 1 2014 2014
dbSNP: rs9839776
rs9839776
4 0.851 0.160 3 181593779 intron variant C/G;T snv 0.800 1.000 1 2014 2014
dbSNP: rs10052957
rs10052957
4 0.851 0.160 5 143407136 non coding transcript exon variant G/A snv 0.28 0.010 1.000 1 2016 2016
dbSNP: rs1800497
rs1800497
56 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 0.010 1.000 1 2016 2016
dbSNP: rs33388
rs33388
12 0.776 0.360 5 143317730 intron variant A/T snv 0.53 0.010 1.000 1 2016 2016
dbSNP: rs41423247
rs41423247
23 0.695 0.440 5 143399010 intron variant G/C snv 0.31 0.010 1.000 1 2016 2016