Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10489177
C1orf112 ; METTL18
0.925 0.120 1 169793666 missense variant T/A;G snv 4.1E-06; 0.19 4
rs104894014
GCK
0.925 0.080 7 44145167 missense variant G/A snv 3
rs1049353
CNR1
0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs10494366
LOC105371475 ; NOS1AP
0.851 0.200 1 162115895 intron variant G/T snv 0.54 7
rs10497721
LOC101927366 ; TMEFF2
1.000 0.040 2 192049636 intron variant C/A;T snv 2
rs1050450
GPX1
0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 43
rs1050828
G6PD
0.790 0.200 X 154536002 missense variant C/T snv 9.1E-03 3.6E-02 15
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 4
rs1052700
PLIN1 ; KIF7
1.000 0.040 15 89665079 3 prime UTR variant A/T snv 0.26 3
rs1056534
FN3K ; TBCD
0.882 0.200 17 82750725 synonymous variant C/A;G;T snv 0.62 5
rs1057293
SGK1
0.925 0.120 6 134172259 synonymous variant G/A snv 0.12 0.11 4
rs1057520504
HNF1A
0.882 0.080 12 120994238 missense variant G/A snv 4
rs1060366
ATP1A1
1.000 0.040 1 116384040 synonymous variant A/G snv 1.3E-03 1.4E-03 2
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs10636
MT2A
0.851 0.160 16 56609431 3 prime UTR variant G/C snv 0.26 7
rs1063856
VWF
0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 14
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
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 6
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
rs10811652
CDKN2B-AS1
0.882 0.120 9 22077086 intron variant A/C;T snv 4
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22