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: rs17249754
rs17249754
12 0.882 0.120 12 89666809 intron variant G/A snv 0.15 0.800 0.929 14 2010 2019
dbSNP: rs11191548
rs11191548
10 0.882 0.080 10 103086421 3 prime UTR variant T/C snv 8.6E-02 0.780 1.000 9 2011 2018
dbSNP: rs2681472
rs2681472
9 0.882 0.080 12 89615182 intron variant A/G snv 0.14 0.860 1.000 8 2009 2019
dbSNP: rs16998073
rs16998073
10 0.925 0.120 4 80263187 upstream gene variant A/G;T snv 0.760 0.857 7 2010 2018
dbSNP: rs1805192
rs1805192
121 0.510 0.840 3 12379739 missense variant C/G snv 0.060 0.667 6 2001 2019
dbSNP: rs3754777
rs3754777
2 1.000 0.040 2 168159404 intron variant C/T snv 0.16 0.060 0.833 6 2012 2019
dbSNP: rs397507444
rs397507444
306 0.405 0.880 1 11794407 missense variant T/G snv 0.060 0.833 6 2008 2015
dbSNP: rs41511344
rs41511344
5 0.882 0.040 4 148152550 stop gained G/A;T snv 0.060 0.833 6 2000 2005
dbSNP: rs1378942
rs1378942
CSK
16 0.790 0.240 15 74785026 intron variant C/A;T snv 0.050 0.800 5 2012 2018
dbSNP: rs1501299
rs1501299
52 0.597 0.720 3 186853334 intron variant G/C;T snv 0.050 0.800 5 2011 2019
dbSNP: rs7119375
rs7119375
2 1.000 0.040 11 57238490 upstream gene variant A/G;T snv 0.050 1.000 5 2009 2016
dbSNP: rs10501367
rs10501367
2 1.000 0.040 11 57238113 upstream gene variant T/C snv 0.73 0.040 1.000 4 2009 2018
dbSNP: rs1468326
rs1468326
1 12 748335 upstream gene variant A/C;T snv 0.040 1.000 4 2005 2018
dbSNP: rs1799998
rs1799998
14 0.742 0.200 8 142918184 upstream gene variant A/G;T snv 0.38 0.040 0.750 4 2010 2019
dbSNP: rs2070744
rs2070744
54 0.608 0.680 7 150992991 intron variant C/T snv 0.70 0.040 1.000 4 2011 2012
dbSNP: rs2576178
rs2576178
9 0.790 0.160 10 88583641 5 prime UTR variant A/G snv 0.29 0.040 0.750 4 2012 2016
dbSNP: rs266729
rs266729
37 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 0.040 1.000 4 2010 2017
dbSNP: rs3761581
rs3761581
5 0.851 0.160 X 129655744 upstream gene variant A/C snv 0.11 0.040 1.000 4 2009 2016
dbSNP: rs3918226
rs3918226
12 0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02 0.040 1.000 4 2012 2015
dbSNP: rs4606
rs4606
16 0.752 0.120 1 192812042 3 prime UTR variant C/G;T snv 0.040 1.000 4 2013 2018
dbSNP: rs776746
rs776746
21 0.724 0.400 7 99672916 splice acceptor variant T/C snv 0.72 0.040 0.500 4 2010 2019
dbSNP: rs9939609
rs9939609
FTO
98 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.040 0.500 4 2010 2013
dbSNP: rs10757274
rs10757274
22 0.701 0.320 9 22096056 intron variant A/G snv 0.41 0.030 0.667 3 2016 2018
dbSNP: rs10757278
rs10757278
44 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.030 1.000 3 2009 2016
dbSNP: rs11174811
rs11174811
2 1.000 12 63146696 3 prime UTR variant C/A snv 0.12 0.030 0.667 3 2011 2019