Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1617640
EPO
0.742 0.520 7 100719675 upstream gene variant C/A;G;T snv 15
rs104894833
RPL36A-HNRNPH2 ; GLA
0.776 0.280 X 101403984 missense variant C/G snv 1.2E-04 1.9E-05 11
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs1317776692
INF2
14 104701619 missense variant C/G;T snv 4.4E-06 1
rs868580411
COL4A5
1.000 X 108602973 missense variant G/A;T snv 2
rs2268388
ACACB
0.851 0.200 12 109205840 intron variant G/A snv 0.14 6
rs267606743
COL4A1
1.000 0.160 13 110192222 missense variant C/T snv 5
rs713041
GPX4
0.776 0.400 19 1106616 stop gained T/A;C snv 4.2E-06; 0.58 16
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs315952
IL1RN
0.763 0.400 2 113132727 missense variant T/A;C snv 4.0E-06; 0.31 10
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 36
rs146956976
GSN
1.000 0.080 9 121302985 missense variant C/T snv 3.1E-04 4.0E-04 2
rs74421874
PSMD9
0.776 0.360 12 121902546 non coding transcript exon variant G/A snv 0.24 14
rs3825172
PSMD9
0.776 0.360 12 121902569 non coding transcript exon variant C/G;T snv 14
rs1043307
PSMD9
0.776 0.360 12 121915890 missense variant A/C;G snv 14
rs5370
EDN1
0.630 0.520 6 12296022 missense variant G/T snv 0.23 0.21 37
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs1191455921
LMX1B
0.925 0.240 9 126693319 missense variant G/A snv 3
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 18
rs3764880
TLR8-AS1 ; TLR8
0.752 0.320 X 12906707 start lost A/G snv 0.31 0.30 11