Disease: Diabetes Mellitus
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10224002
PRKAG2
0.925 0.080 7 151717955 intron variant A/G snv 0.31 12
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs1037733674
GCG ; LOC101929532
0.882 0.120 2 162147429 missense variant T/C snv 1.4E-05 5
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs10494366
LOC105371475 ; NOS1AP
0.851 0.200 1 162115895 intron variant G/T snv 0.54 7
rs10509291 0.827 0.280 10 67875446 downstream gene variant T/A snv 7.1E-02 6
rs1057520504
HNF1A
0.882 0.080 12 120994238 missense variant G/A snv 4
rs10636
MT2A
0.851 0.160 16 56609431 3 prime UTR variant G/C snv 0.26 7
rs1073203 0.882 0.160 5 125983763 intron variant C/G snv 0.15 4
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs10757283 0.827 0.120 9 22134173 intergenic variant C/A;T snv 0.45 6
rs10761600
ARID5B
0.925 0.120 10 61997361 intron variant A/G;T snv 3
rs10767664
BDNF
0.752 0.400 11 27704439 intron variant T/A snv 0.83 16
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 27
rs10885390 0.925 0.080 10 112881038 regulatory region variant T/A snv 0.30 3
rs10911021
LOC105371642 ; LINC01344
0.807 0.160 1 182112825 intron variant C/T snv 0.36 11
rs10946398
CDKAL1
0.827 0.160 6 20660803 intron variant A/C snv 0.40 7
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27
rs11196205
TCF7L2
0.827 0.200 10 113047288 intron variant G/A;C;T snv 7
rs11212617
C11orf65
0.827 0.200 11 108412434 intron variant C/A snv 0.49 7
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs11771443
NOS3
0.790 0.360 7 150990599 upstream gene variant C/T snv 0.16 8