Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 22
rs5068
NPPA ; NPPA-AS1 ; CLCN6
0.776 0.160 1 11845917 3 prime UTR variant A/G;T snv 13
rs198358
NPPA-AS1 ; CLCN6
0.925 0.040 1 11844019 3 prime UTR variant T/C snv 0.32 4
rs78314028
CYTH3
1.000 0.040 7 6163445 3 prime UTR variant C/A snv 2.2E-02 3
rs10932374
ERBB4
0.925 0.040 2 211379678 3 prime UTR variant G/A snv 0.23 2
rs13003941
ERBB4
0.925 0.040 2 211378978 3 prime UTR variant G/C;T snv 0.26 2
rs1595064
ERBB4
0.925 0.040 2 211378020 3 prime UTR variant G/A;C snv 2
rs1595065
ERBB4
0.925 0.040 2 211377916 3 prime UTR variant G/A snv 0.73 2
rs3748960
ERBB4
0.925 0.040 2 211383109 3 prime UTR variant C/T snv 0.96 2
rs3829365
POSTN
0.925 0.040 13 37598759 5 prime UTR variant G/A;C snv 4.0E-06; 0.11 3
rs5443
CDCA3 ; GNB3
0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs4898
TIMP1 ; SYN1 ; MIR4769
0.672 0.520 X 47585586 synonymous variant T/C snv 0.46 0.46 25
rs737337
DOCK6
0.925 0.040 19 11236817 synonymous variant T/C snv 0.15 0.20 6
rs1429117513
LAG3
0.925 0.040 12 6775316 synonymous variant T/C snv 4.0E-06 2
rs1805126
SCN5A
0.925 0.040 3 38550915 synonymous variant A/G snv 0.39 0.44 2
rs6123837
GNAS ; LOC101927932
0.925 0.040 20 58890516 synonymous variant G/A snv 0.30 2
rs28362491
LOC105377621 ; NFKB1
0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs2074755
BAZ1B
0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 20
rs261332
ALDH1A2 ; LIPC-AS1 ; LIPC
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 20
rs911119
CST3
0.807 0.120 20 23632100 non coding transcript exon variant C/G;T snv 9
rs8105292
LINC01782
1.000 0.040 19 32103916 non coding transcript exon variant T/C snv 0.19 3
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131