Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs545854 0.882 0.160 8 10002570 intron variant G/C snv 0.85 4
rs7826222 1.000 0.080 8 10002570 intron variant G/C snv 1
rs757139012
SIM1
0.882 0.080 6 100390522 missense variant T/C snv 8.0E-06; 4.0E-06 1.4E-05 3
rs3734354
SIM1 ; LOC102724406
1.000 0.080 6 100420903 missense variant G/A;T snv 1.6E-04; 0.18 2
rs756633599
SIM1
0.925 0.080 6 100447299 missense variant G/A snv 1.6E-05 2
rs3213541
SIM1
1.000 0.080 6 100448367 intron variant A/G;T snv 1
rs10895068
PGR ; PGR-AS1
0.752 0.240 11 101129483 5 prime UTR variant C/T snv 3.6E-02 14
rs763351020
SERPINE1
0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 35
rs35400704
VGF
1.000 0.080 7 101163271 stop gained C/A;G;T snv 6.4E-06 1
rs2228611
DNMT1
0.708 0.520 19 10156401 synonymous variant T/A;C snv 0.52 19
rs7973796
HELLPAR
1.000 0.080 12 102202345 non coding transcript exon variant G/A snv 0.56 2
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs782656324
CUX1
0.925 0.120 7 102273394 missense variant C/G;T snv 8.1E-06 2
rs6219
HELLPAR ; LINC02456 ; IGF1
1.000 0.080 12 102396414 3 prime UTR variant C/T snv 8.9E-02 2
rs6214
LINC02456 ; HELLPAR ; IGF1
0.672 0.400 12 102399791 3 prime UTR variant C/T snv 0.45 26
rs2293225
IL18RAP
0.925 0.200 2 102419429 intron variant C/T snv 0.16 2
rs2272127
IL18RAP
1.000 0.080 2 102423413 intron variant C/G snv 0.22 3
rs7559479
IL18RAP
1.000 0.080 2 102452327 3 prime UTR variant G/A snv 0.78 1
rs35767
IGF1 ; LOC105369944
0.763 0.360 12 102481791 upstream gene variant A/C;G;T snv 13
rs679620
MMP3
0.716 0.360 11 102842889 missense variant T/C snv 0.58 0.57 17
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs4684677
GHRLOS ; GHRL
0.742 0.360 3 10286769 missense variant T/A snv 0.10 6.6E-02 13
rs2075356
GHRL ; GHRLOS
0.882 0.160 3 10287125 non coding transcript exon variant T/C snv 8.3E-02 5
rs1422753499
MMP12
0.925 0.120 11 102873034 missense variant T/C;G snv 7.0E-06 2
rs696217
GHRL ; GHRLOS
0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 32