Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5370
EDN1
0.630 0.520 6 12296022 missense variant G/T snv 0.23 0.21 37
rs587782951
JPH2
0.807 0.080 20 44160305 missense variant G/T snv 6
rs1337916669
LOC108783645 ; HFE
0.925 0.040 6 26092879 missense variant G/T snv 2
rs452159
ADA
1.000 0.040 20 44642461 intron variant G/T snv 0.28 2
rs9885413 0.925 0.040 5 110840429 intergenic variant G/T snv 0.19 2
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs13003941
ERBB4
0.925 0.040 2 211378978 3 prime UTR variant G/C;T snv 0.26 2
rs2241562
HRH2
0.925 0.040 5 175684809 intron variant G/C;T snv 1.0E-03 2
rs1801253
ADRB1
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 34
rs1022113606
SOD3
0.732 0.280 4 24800161 missense variant G/C snv 1.6E-04 2.1E-05 17
rs1800437
GIPR
0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 13
rs121918090
TTR
0.790 0.240 18 31593026 missense variant G/C snv 8
rs398122917
CLIC2
0.882 0.080 X 155280059 missense variant G/C snv 4.4E-05 1.1E-04 5
rs1553265736
LMNA
0.925 0.040 1 156136080 missense variant G/C snv 4
rs899115126
EDNRA
0.882 0.080 4 147542603 missense variant G/C snv 3
rs958546
LRRC63
0.882 0.040 13 46259582 intron variant G/C snv 0.29 3
rs9303504
PRKCA
0.925 0.040 17 66319248 intron variant G/C snv 0.59 2
rs1009388
POMC
1.000 0.040 2 25168232 intron variant G/C snv 0.18 1
rs8193037
IL17A
0.752 0.320 6 52186311 upstream gene variant G/A;T snv 12
rs766265889
TTN-AS1 ; TTN
0.827 0.240 2 178535508 stop gained G/A;T snv 8.0E-06; 4.0E-06 11
rs7626962
SCN5A
0.790 0.080 3 38579416 missense variant G/A;T snv 1.6E-05; 5.9E-03 10
rs3766871
RYR2
0.790 0.240 1 237614784 missense variant G/A;T snv 4.0E-02 9
rs121918080
TTR
0.827 0.240 18 31595128 missense variant G/A;T snv 2.4E-05 6
rs371401403
MYBPC3
0.807 0.080 11 47335996 missense variant G/A;T snv 6.8E-05; 7.9E-05 6
rs765545512
HFE
0.827 0.240 6 26093226 missense variant G/A;T snv 4.0E-06; 1.6E-05 6