Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs756322971
CASR
0.763 0.240 3 122284955 missense variant C/A;G snv 9
rs75444904
HPR ; TXNL4B
0.851 0.160 16 72061751 intron variant A/C snv 2.4E-02 4
rs753350907
PAX2
0.827 0.080 10 100806499 missense variant G/A;C;T snv 4.0E-06; 4.0E-06 5
rs752390951
KLK4
0.925 0.080 19 50908408 missense variant G/T snv 8.0E-06 7.0E-06 2
rs7490924
EFNB2
0.925 0.080 13 106519396 non coding transcript exon variant A/G snv 0.51 2
rs743811 0.882 0.160 22 35396981 upstream gene variant T/A;C snv 4
rs74315342
NPHS2
0.763 0.120 1 179561327 missense variant C/T snv 6.0E-04 5.3E-04 10
rs73885319
APOL1
0.851 0.120 22 36265860 missense variant A/G snv 1.6E-02 6.6E-02 6
rs730947 0.925 0.080 2 218838575 upstream gene variant A/C snv 1.0E-01 2
rs730497
GCK ; LOC105375257
0.882 0.160 7 44184122 intron variant G/A snv 0.17 4
rs702483
RAC1
0.925 0.080 7 6387310 intron variant C/A;T snv 0.54 2
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs696
NFKBIA
0.708 0.520 14 35401887 3 prime UTR variant C/T snv 0.45 22
rs6954996
RAC1
0.925 0.080 7 6401627 non coding transcript exon variant G/A;T snv 2
rs6936632
CD2AP
0.925 0.080 6 47588297 intron variant G/A snv 7.6E-02 2
rs6280
DRD3
0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs61752717
MEFV
0.583 0.840 16 3243407 missense variant T/A;C snv 2.8E-04 72
rs61747728
NPHS2
0.701 0.240 1 179557079 missense variant C/T snv 3.0E-02 2.8E-02 20
rs60910145
APOL1
0.851 0.120 22 36265988 missense variant T/G snv 1.6E-02 6.6E-02 5
rs5743708
TLR2
0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs5742909
CTLA4
0.614 0.680 2 203867624 upstream gene variant C/T snv 6.7E-02 40
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs5443
CDCA3 ; GNB3
0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs5370
EDN1
0.630 0.520 6 12296022 missense variant G/T snv 0.23 0.21 37
rs5355
C1orf112 ; SELE
0.742 0.240 1 169726729 missense variant G/A snv 4.5E-02 3.3E-02 14