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: rs7903146
rs7903146
93 0.554 0.680 10 112998590 intron variant C/G;T snv 0.800 1.000 9 2012 2019
dbSNP: rs8050136
rs8050136
FTO
32 0.716 0.560 16 53782363 intron variant C/A snv 0.40 0.800 1.000 5 2009 2019
dbSNP: rs780094
rs780094
62 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.800 1.000 3 2012 2019
dbSNP: rs10248619
rs10248619
2 7 50683393 intron variant T/C snv 0.71 0.800 1.000 1 2012 2012
dbSNP: rs10830963
rs10830963
27 0.776 0.400 11 92975544 intron variant C/G snv 0.22 0.800 1.000 1 2012 2012
dbSNP: rs10885122
rs10885122
4 1.000 0.080 10 111282335 intergenic variant T/G snv 0.71 0.800 1.000 1 2012 2012
dbSNP: rs11041816
rs11041816
2 11 8222251 downstream gene variant A/G snv 0.36 0.800 1.000 1 2012 2012
dbSNP: rs11558471
rs11558471
5 1.000 0.080 8 117173494 3 prime UTR variant A/G snv 0.25 0.800 1.000 1 2012 2012
dbSNP: rs11603334
rs11603334
5 1.000 0.080 11 72721940 5 prime UTR variant G/A snv 0.12 0.800 1.000 1 2012 2012
dbSNP: rs11605924
rs11605924
5 1.000 0.080 11 45851540 intron variant A/C snv 0.39 0.800 1.000 1 2012 2012
dbSNP: rs11708067
rs11708067
9 0.882 0.080 3 123346931 intron variant A/G snv 0.19 0.800 1.000 1 2012 2012
dbSNP: rs11920090
rs11920090
5 1.000 0.040 3 170999732 intron variant T/A snv 0.20 0.800 1.000 1 2012 2012
dbSNP: rs13179048
rs13179048
2 5 96207022 intron variant C/A snv 0.23 0.800 1.000 1 2012 2012
dbSNP: rs1371614
rs1371614
3 2 26930006 intron variant C/T snv 0.29 0.800 1.000 1 2012 2012
dbSNP: rs1470579
rs1470579
5 0.925 0.160 3 185811292 intron variant A/C snv 0.46 0.800 1.000 1 2012 2012
dbSNP: rs1483121
rs1483121
4 1.000 0.080 11 48311808 downstream gene variant G/A snv 9.7E-02 0.800 1.000 1 2012 2012
dbSNP: rs174550
rs174550
13 0.925 0.160 11 61804006 5 prime UTR variant T/C snv 0.28 0.800 1.000 1 2012 2012
dbSNP: rs2191349
rs2191349
4 1.000 0.080 7 15024684 intergenic variant G/T snv 0.54 0.800 1.000 1 2012 2012
dbSNP: rs2293941
rs2293941
2 13 27917061 intron variant G/A snv 0.23 0.800 1.000 1 2012 2012
dbSNP: rs2714337
rs2714337
2 6 7240344 intron variant A/T snv 0.34 0.800 1.000 1 2012 2012
dbSNP: rs340874
rs340874
7 0.882 0.080 1 213985913 non coding transcript exon variant T/C snv 0.40 0.800 1.000 1 2012 2012
dbSNP: rs3736594
rs3736594
3 2 27772914 intron variant A/C snv 0.62 0.800 1.000 1 2012 2012
dbSNP: rs4607517
rs4607517
GCK
8 0.882 0.080 7 44196069 intron variant G/A;C snv 0.800 1.000 1 2012 2012
dbSNP: rs4841132
rs4841132
14 8 9326086 non coding transcript exon variant A/G snv 0.89 0.800 1.000 1 2012 2012
dbSNP: rs560887
rs560887
18 0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 0.800 1.000 1 2012 2012