Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8321
ZNRD1
0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 16
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs1715
ZNF615
0.851 0.040 19 51991525 3 prime UTR variant T/C snv 1.4E-05 5
rs9297357
ZFPM2 ; LOC105375695
0.851 0.040 8 105130105 intron variant C/G;T snv 5
rs6736411
WDPCP
0.925 0.120 2 63446926 intron variant G/A snv 0.78 2
rs9566845
VWA8
0.925 0.040 13 41761944 intron variant G/A snv 6.1E-02 3
rs1701137
VPS53
0.882 0.080 17 572682 intron variant C/T snv 0.50 3
rs386834070
VPS13B
0.851 0.360 8 99134644 stop gained C/T snv 9
rs2097603
TXNRD2 ; COMT
0.882 0.040 22 19940569 intron variant G/A;T snv 3
rs201391000
TXNRD2
0.925 0.080 22 19877157 missense variant C/A;T snv 2.3E-04 2
rs2303380
TTC12
1.000 0.040 11 113329987 splice region variant G/A snv 0.61 0.64 2
rs1538979
TSNAX-DISC1 ; DISC1
0.882 0.160 1 231761122 intron variant C/T snv 0.19 3
rs2021722
TRIM26
0.851 0.040 6 30206354 intron variant C/A;T snv 0.24 5
rs4570625
TPH2
0.724 0.200 12 71938143 upstream gene variant G/T snv 0.27 25
rs1843809
TPH2
0.851 0.080 12 71954918 intron variant G/T snv 0.77 6
rs11178997
TPH2
0.827 0.040 12 71938373 upstream gene variant T/A snv 0.12 5
rs17110690
TPH2
0.925 0.080 12 72014217 intron variant G/A snv 0.19 2
rs1114167296
TMEM47
0.827 0.160 X 34656995 missense variant C/G snv 6
rs534654
TMEM165
0.925 0.040 4 55424053 non coding transcript exon variant A/G snv 0.81 2
rs121918695
THRB
0.882 0.080 3 24127696 missense variant C/T snv 4.0E-06 3
rs12576775
TENM4
0.827 0.080 11 79366149 intron variant A/G snv 0.15 6
rs11152369
TCF4
0.851 0.040 18 55399097 intron variant A/C snv 6.3E-02 5
rs1569110700
TCF20
0.925 0.080 22 42179633 missense variant G/A snv 5
rs1307997067
TAX1BP3 ; P2RX5-TAX1BP3
0.851 0.320 17 3664199 missense variant A/C;G snv 4.0E-06 7.0E-06 7
rs7089973
TAF9BP2 ; ABLIM1
0.925 0.040 10 114809806 intron variant C/A snv 0.41 2