Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1050828
G6PD
0.790 0.200 X 154536002 missense variant C/T snv 9.1E-03 3.6E-02 15
rs518147
HTR2C
0.807 0.200 X 114584109 5 prime UTR variant C/A;G snv 7
rs12836771
HTR2C ; MIR1912 ; MIR1264
0.882 0.080 X 114650913 intron variant A/G snv 0.12 4
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs1375557127
HNF4A
0.925 0.080 20 44424123 missense variant G/A snv 4.0E-06 2
rs1385251852
MIR3646 ; HNF4A
0.925 0.080 20 44406208 frameshift variant G/- delins 2
rs1392795567
HNF4A
0.925 0.080 20 44414663 splice donor variant G/A snv 2
rs1568724014
MIR3646 ; HNF4A
0.925 0.080 20 44407421 stop gained C/T snv 2
rs1018185646
HNF4A
1.000 0.040 20 44428455 missense variant T/C snv 4.0E-06 1
rs1410713 1.000 0.040 20 3079704 downstream gene variant A/C snv 0.62 1
rs2282018
AVP
1.000 0.040 20 3084303 intron variant C/T snv 0.60 1
rs2770381 1.000 0.040 20 3081340 downstream gene variant A/C snv 0.35 1
rs6084264
AVP
1.000 0.040 20 3089925 upstream gene variant T/C snv 0.58 1
rs369841551
MC4R
0.882 0.120 18 60371884 stop gained G/A;T snv 4.0E-06 3
rs146488435
KCNH6
0.851 0.080 17 63533914 missense variant C/G;T snv 8.0E-06; 6.4E-05 5
rs8066560
SREBF1
0.925 0.040 17 17824729 intron variant A/G snv 0.64 2
rs9906827
RPTOR
0.925 0.120 17 80691605 intron variant C/A;T snv 2
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 21
rs572115942
PHKG2
0.925 0.240 16 30756714 missense variant G/A snv 8.0E-05 7.7E-05 7
rs1320702652
MFAP1
0.752 0.160 15 43824536 missense variant G/A snv 4.0E-06 11
rs11549465
HIF1A-AS3 ; HIF1A
0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs4644
LGALS3
0.732 0.320 14 55138217 missense variant C/A;G snv 0.35 14
rs8004664
FOXN3
0.925 0.080 14 89568628 intron variant G/A;C snv 3
rs10139403
DLK1
1.000 0.040 14 100728224 intron variant A/G snv 0.62 1