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: rs6296
rs6296
23 0.732 0.160 6 77462543 synonymous variant C/G snv 0.31 0.27 0.020 1.000 2 2001 2002
dbSNP: rs495225
rs495225
4 0.882 0.040 3 172448243 synonymous variant G/A;C;T snv 0.66 0.010 1.000 1 2006 2006
dbSNP: rs554073050
rs554073050
CCK
3 0.925 0.040 3 42263460 synonymous variant G/A snv 1.2E-05 7.0E-06 0.010 1.000 1 2006 2006
dbSNP: rs696217
rs696217
32 0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 0.010 1.000 1 2006 2006
dbSNP: rs746682028
rs746682028
36 0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 0.010 1.000 1 2006 2006
dbSNP: rs6265
rs6265
272 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.020 1.000 2 2006 2007
dbSNP: rs759834365
rs759834365
237 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 0.020 1.000 2 2006 2007
dbSNP: rs1049353
rs1049353
42 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 0.010 1.000 1 2009 2009
dbSNP: rs4633
rs4633
25 0.695 0.400 22 19962712 synonymous variant C/T snv 0.46 0.45 0.010 1.000 1 2011 2011
dbSNP: rs4818
rs4818
27 0.683 0.440 22 19963684 synonymous variant C/G;T snv 0.34 0.010 1.000 1 2011 2011
dbSNP: rs1800497
rs1800497
56 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 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: rs142014203
rs142014203
1 1.000 0.040 8 62346358 intron variant T/G snv 2.1E-02 0.800 1.000 1 2013 2013
dbSNP: rs1445130
rs1445130
1 1.000 0.040 2 18653385 regulatory region variant A/G snv 0.12 0.800 1.000 1 2013 2013
dbSNP: rs77600076
rs77600076
1 1.000 0.040 21 18159125 intron variant A/C snv 2.5E-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: rs52820871
rs52820871
6 0.827 0.160 18 60371599 missense variant T/G snv 6.9E-03 7.6E-03 0.010 < 0.001 1 2015 2015
dbSNP: rs53576
rs53576
42 0.641 0.320 3 8762685 intron variant A/G;T snv 0.010 1.000 1 2015 2015
dbSNP: rs4680
rs4680
249 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 0.040 1.000 4 2011 2017
dbSNP: rs12490016
rs12490016
3 0.882 0.120 3 157121142 intron variant G/C snv 4.6E-02 0.010 1.000 1 2017 2017
dbSNP: rs1630623
rs1630623
3 0.882 0.120 9 72725323 intron variant A/G snv 0.29 0.010 1.000 1 2017 2017
dbSNP: rs200889048
rs200889048
3 0.882 0.120 3 74928276 intergenic variant C/- del 0.010 1.000 1 2017 2017
dbSNP: rs287103
rs287103
1 1.000 0.040 19 33801816 intron variant A/G snv 0.67 0.010 1.000 1 2017 2017