Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11465804
IL23R
0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 10
rs3024505 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 10
rs2205960
TNFSF4
0.763 0.400 1 173222336 intergenic variant G/A;T snv 9
rs200890679
MTHFR
0.790 0.240 1 11795191 missense variant C/A;G snv 1.8E-04 2.0E-04 7
rs3748816
MMEL1
0.827 0.200 1 2595307 missense variant A/G snv 0.41 0.46 7
rs3761959
FCRL3
0.827 0.320 1 157699488 intron variant C/A;G;T snv 7
rs6790
GAS5 ; SNORD47 ; SNORD78 ; SNORD79 ; SNORD81 ; SNORD80 ; SNORD44
0.790 0.320 1 173865494 non coding transcript exon variant G/A snv 8.9E-02 7
rs2274910
ITLN1
0.827 0.200 1 160882256 non coding transcript exon variant T/C snv 0.65 0.58 6
rs10797431
LOC100996583
0.851 0.080 1 2569783 non coding transcript exon variant G/T snv 0.42 5
rs10903122 0.882 0.200 1 24977085 intergenic variant A/G snv 0.56 5
rs11584383
MROH3P
0.827 0.200 1 200966738 downstream gene variant T/C snv 0.24 5
rs17368528
H6PD
0.827 0.400 1 9264154 missense variant C/A;T snv 0.12 8.9E-02 5
rs2816316
LOC105371664
0.882 0.200 1 192567683 intron variant C/A snv 0.79 5
rs296547
MROH3P
0.882 0.200 1 200923009 intron variant T/C snv 0.53 5
rs4085613 0.827 0.160 1 152577542 downstream gene variant T/G snv 0.59 5
rs55829688
SNORD77 ; SNORA103 ; ZBTB37 ; SNORD76 ; SNORD74 ; SNORD75 ; GAS5
0.827 0.200 1 173868168 5 prime UTR variant T/C;G snv 5
rs5938
PTAFR
0.827 0.200 1 28150351 missense variant G/T snv 8.0E-03 2.5E-03 5
rs11586238 0.925 0.160 1 116720516 regulatory region variant C/G snv 0.19 4
rs368311455
CPT2
0.882 0.200 1 53211185 missense variant C/T snv 3.2E-05 2.8E-05 4
rs5368
SELE ; C1orf112
0.882 0.160 1 169727805 missense variant G/A snv 0.14 0.11 4
rs6133
SELP
0.851 0.280 1 169596108 missense variant C/A;G snv 0.12 4
rs9286879 0.851 0.200 1 172893094 intron variant A/G snv 0.32 4
rs945635
FCRL3
0.882 0.200 1 157700500 5 prime UTR variant C/A;G snv 5.6E-05; 0.45 4
rs10800309 0.925 0.120 1 161502368 upstream gene variant A/G;T snv 3
rs1323292
LOC105371664
0.882 0.160 1 192571891 intron variant G/A snv 0.86 3