Disease: Diabetes Mellitus
Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1004446
IGF2 ; INS-IGF2 ; IGF2-AS
0.827 0.240 11 2148913 intron variant G/A snv 0.37 5
rs10116772
GLIS3
0.882 0.080 9 4290541 intron variant C/A;T snv 2
rs1013773109
GRB14
1.000 0.040 2 164497436 missense variant T/C snv 2.1E-05 2
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 59
rs1036915
NTRK2
1.000 0.040 9 84822934 intron variant A/G snv 0.40 2
rs1037733674
GCG ; LOC101929532
0.882 0.120 2 162147429 missense variant T/C snv 1.4E-05 5
rs1042488900
ATF6
1.000 0.040 1 161802188 synonymous variant C/T snv 2
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 25
rs10484821
LOC105378024
1.000 0.040 6 139547773 intron variant T/C snv 0.15 2
rs10486567
JAZF1
0.851 0.120 7 27936944 intron variant G/A snv 0.28 8
rs104894014
GCK
0.925 0.080 7 44145167 missense variant G/A snv 2
rs10494366
LOC105371475 ; NOS1AP
0.851 0.200 1 162115895 intron variant G/T snv 0.54 6
rs10509291 0.827 0.280 10 67875446 downstream gene variant T/A snv 7.1E-02 6
rs10517086
LINC02357
0.882 0.160 4 26083889 intron variant G/A snv 0.27 2
rs1052700
PLIN1 ; KIF7
1.000 0.040 15 89665079 3 prime UTR variant A/T snv 0.26 3
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 32
rs10747983
AVPR1A
1.000 0.040 12 63144678 3 prime UTR variant G/A snv 0.29 2
rs10757272
CDKN2B-AS1
0.851 0.160 9 22088261 intron variant C/T snv 0.41 3
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41 20
rs10757283 0.827 0.120 9 22134173 intergenic variant C/A;T snv 0.45 6
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 19
rs10818684 1.000 0.040 9 122407651 intron variant C/T snv 0.62 2