Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10038177
WDR36
0.925 0.040 5 111100751 intron variant C/T snv 0.53 0.54 3
rs10120688
CDKN2B-AS1
0.807 0.080 9 22056500 intron variant G/A snv 0.50 7
rs1013278 1.000 0.040 7 117963766 regulatory region variant G/A;C snv 1
rs1015213 0.851 0.040 8 51974981 intron variant C/T snv 0.14 6
rs10152898 1.000 0.040 15 73962780 intergenic variant G/A;T snv 1
rs1020338837
AZI2
1.000 0.040 3 28340470 missense variant T/C;G snv 4.0E-06 1
rs10281637 1.000 0.040 7 116511284 downstream gene variant T/C snv 0.28 2
rs1035650739
LOC105372437 ; NAPSA ; NR1H2
1.000 0.040 19 50362252 missense variant C/G;T snv 4.0E-06 1
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1042713
ADRB2
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs10483727 0.851 0.040 14 60606157 upstream gene variant T/C snv 0.45 4
rs1048661
LOXL1-AS1 ; LOXL1
0.732 0.320 15 73927205 missense variant G/T snv 0.33 0.28 14
rs10505100
ANGPT1
1.000 0.040 8 107266388 intron variant C/A snv 0.13 1
rs1057518844
CREBBP
1.000 0.040 16 3757288 missense variant C/T snv 2
rs1057518956
ZEB1
0.925 0.080 10 31520308 stop gained C/T snv 3
rs1063192
CDKN2B ; CDKN2B-AS1
0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv 24
rs10918274
TMCO1
1.000 0.040 1 165745179 intron variant T/C snv 0.89 2
rs10965219
CDKN2B-AS1
0.882 0.080 9 22053688 intron variant A/G snv 0.58 4
rs11024102
PLEKHA7
0.851 0.040 11 16987058 intron variant T/C snv 0.20 7
rs11217878
ARHGEF12
1.000 0.040 11 120469674 intron variant G/A snv 0.20 2
rs11258194
OPTN
0.776 0.160 10 13110400 missense variant T/A snv 4.4E-02 6.0E-02 9
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs113432289
RAPGEF5
1.000 0.040 7 22253498 intron variant A/C snv 3.3E-03 1
rs113985657
EXOC2
1.000 0.040 6 597203 intron variant C/T snv 0.14 2
rs116529882
WDR36
0.925 0.040 5 111110280 missense variant G/A snv 7.5E-04 8.9E-04 2