Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7713317
LOC101929710
5 96381018 intron variant A/G snv 0.28 3
rs4869272
MIR583HG ; LOC101929710
5 96203744 intron variant C/T snv 0.72 3
rs2605627
SMCO4
11 93526349 intron variant A/G snv 0.79 2
rs11782386 8 9344277 intron variant C/T snv 9.7E-02 2
rs2126259
LOC157273
1.000 8 9327636 intron variant T/C snv 0.87 9
rs983309 8 9320222 intron variant T/G snv 0.82 2
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 27
rs1387153 0.807 0.200 11 92940662 downstream gene variant C/G;T snv 10
rs8020333
FOXN3
14 89568505 intron variant C/G;T snv 0.52 2
rs7708285
ZBED3-AS1
1.000 0.080 5 77130042 intron variant G/A snv 0.76 3
rs1783598
FCHSD2
1.000 0.080 11 73140418 intron variant C/G;T snv 3
rs1552224
ARAP1
1.000 0.080 11 72722053 5 prime UTR variant A/C snv 0.12 4
rs11603334
ARAP1
1.000 0.080 11 72721940 5 prime UTR variant G/A snv 0.12 5
rs3778321
RREB1
6 7250037 3 prime UTR variant G/A snv 0.11 2
rs17762454
RREB1
0.925 0.120 6 7212967 non coding transcript exon variant C/T snv 0.25 4
rs1983127
HKDC1 ; LOC101928994
10 69230145 intron variant G/T snv 0.38 2
rs4458523
WFS1
1.000 0.080 4 6288259 intron variant T/G snv 0.61 3
rs12440695 15 62142957 regulatory region variant T/C snv 0.32 3
rs4775471 15 62132450 intergenic variant C/T snv 0.18 2
rs4502156 1.000 0.080 15 62090956 intergenic variant T/C snv 0.55 4
rs2851682
FADS2
11 61848540 intron variant A/G snv 9.9E-02 5
rs174583
FADS2
0.807 0.320 11 61842278 intron variant C/T snv 0.35 16
rs174576
FADS2
0.851 0.200 11 61836038 intron variant C/A;T snv 14
rs174550
FADS1 ; FADS2
0.925 0.160 11 61804006 5 prime UTR variant T/C snv 0.28 13
rs174537
TMEM258 ; MYRF
0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 23