Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6474387
IKBKB
0.882 0.080 8 42328734 intron variant T/C snv 0.76 3
rs6598964
LIN28A
0.882 0.080 1 26419836 intron variant A/G snv 0.67 3
rs10958713
IKBKB
0.925 0.080 8 42323198 intron variant C/T snv 0.28 2
rs11923427
RAF1
0.925 0.080 3 12622336 intron variant C/G;T snv 2
rs12485716
CASR
0.925 0.080 3 122260843 intron variant G/A snv 0.36 2
rs12497343
MYLKP1 ; LOC105377207
0.925 0.080 3 75330074 intron variant C/G;T snv 2
rs17250717
CASR
0.925 0.080 3 122261339 intron variant G/T snv 7.4E-02 2
rs1967327
PRKRA ; PJVK
0.925 0.080 2 178449632 intron variant G/A;C;T snv 2
rs2470144
CYP19A1
0.925 0.080 15 51329528 intron variant T/C snv 0.60 2
rs283415
ADH1C ; ADH1B
0.925 0.080 4 99349450 intron variant C/T snv 0.64 2
rs374400
OBSCN
0.925 0.080 1 228347383 intron variant C/T snv 0.40 2
rs3804592
CASR
0.925 0.080 3 122260382 intron variant G/A snv 0.18 2
rs3811802
ADH1B
0.925 0.080 4 99323064 intron variant A/C;G;T snv 2
rs4548444
MAPKAPK2
0.925 0.080 1 206716793 intron variant A/G snv 0.20 2
rs4678174
CASR
0.925 0.080 3 122282024 intron variant C/T snv 0.56 2
rs5029748
IKBKB
0.925 0.080 8 42283031 intron variant G/T snv 0.22 2
rs8039880
MAP2K1
0.925 0.080 15 66468004 intron variant A/G snv 0.21 2
rs9694958
IKBKB ; LOC105379395
0.925 0.080 8 42298528 intron variant A/G snv 0.26 2
rs12527379 1.000 0.080 6 131958700 intron variant G/A snv 0.31 1
rs16892766 0.716 0.240 8 116618444 intergenic variant A/C snv 9.3E-02 18
rs4779584 0.732 0.160 15 32702555 intergenic variant T/C snv 0.67 16
rs961253 0.732 0.240 20 6423634 intergenic variant C/A snv 0.34 15
rs719725 0.827 0.080 9 6365683 intergenic variant A/C snv 0.34 7
rs6854845 0.827 0.080 4 74821455 intergenic variant G/T snv 0.13 6
rs1365611 0.925 0.080 4 174462542 intergenic variant C/T snv 0.28 2