Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10012
CYP1B1 ; CYP1B1-AS1
0.716 0.280 2 38075247 missense variant G/C snv 0.31 0.36 16
rs1002481
REV3L ; MFSD4B
0.882 0.080 6 111390819 intron variant T/A;G snv 3
rs10036653
ATG10
0.851 0.160 5 81970563 upstream gene variant A/T snv 0.17 4
rs10040363
XRCC4
0.882 0.080 5 83177826 intron variant A/G snv 0.50 3
rs10053847
IL7R
0.882 0.080 5 35878038 3 prime UTR variant G/A snv 0.13 3
rs10054203
TERT
0.882 0.080 5 1279849 intron variant G/A;C;T snv 3
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs10079250
CSF1R
0.827 0.120 5 150070569 missense variant T/C snv 9.9E-02 8.6E-02 7
rs1014264982
HMG20B
0.882 0.080 19 3577038 missense variant G/A;C snv 6.8E-06 7.0E-06 3
rs10187911
NRXN1
0.882 0.080 2 50420809 intron variant C/A;G;T snv 3
rs1019340046
TP53
0.882 0.080 17 7674225 missense variant C/T snv 5
rs10213865
LOC105374724 ; IL7R
0.827 0.120 5 35857748 intron variant A/C;T snv 5
rs10244817
POT1
0.882 0.080 7 124827416 intron variant T/C snv 0.22 3
rs10254120
PMS2
0.851 0.080 7 6005996 missense variant C/A;G;T snv 7.2E-02 5
rs1026411
LOC105375751 ; PCAT1
0.827 0.080 8 127014165 intron variant G/A;C snv 0.25 5
rs1035938
BICRA
0.776 0.120 19 47680514 missense variant C/G;T snv 0.29 8
rs10412613
PPP2R1A
0.882 0.080 19 52209575 intron variant G/A snv 0.63 3
rs1041983
NAT2
0.732 0.240 8 18400285 synonymous variant C/T snv 0.34 0.36 15
rs1042028
SULT1A1
0.658 0.440 16 28606193 missense variant C/T snv 0.22 0.30 30
rs10421768
HAMP
0.807 0.120 19 35281996 intron variant A/G snv 0.21 6
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1042711
ADRB2
0.827 0.120 5 148826785 5 prime UTR variant C/A;G;T snv 4.2E-06; 0.68 5
rs1043973338
IL1B
0.882 0.080 2 112830483 missense variant A/C snv 3
rs1043994
NOTCH3
0.827 0.120 19 15192033 synonymous variant T/A;C snv 4.0E-06; 0.85 7
rs1044396
CHRNA4
0.742 0.240 20 63349782 missense variant G/A;C snv 0.47; 6.1E-05 17