Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6801957
SCN10A
1.000 0.080 3 38725824 intron variant T/C snv 0.67 7
rs9391858
TSBP1-AS1 ; TSBP1
0.925 0.080 6 32373621 intron variant A/G snv 0.13 6
rs10797431
LOC100996583
0.851 0.080 1 2569783 non coding transcript exon variant G/T snv 0.42 5
rs1449263 1.000 0.080 2 181454574 upstream gene variant C/T snv 0.56 5
rs3094609
HCG27
0.925 0.080 6 31197789 non coding transcript exon variant T/C snv 0.86 0.89 5
rs3130558
PSORS1C1
0.925 0.080 6 31129406 intron variant C/G snv 0.77 5
rs3130975
C6orf15 ; PSORS1C1
0.925 0.080 6 31114061 upstream gene variant C/T snv 0.27 5
rs3130981
CDSN ; PSORS1C1
0.925 0.080 6 31116036 missense variant T/C;G snv 0.76 5
rs3131009
PSORS1C1
0.925 0.080 6 31131055 intron variant G/A;C snv 5
rs528878831
PSORS1C1
0.925 0.080 6 31131055 intron variant G/A;C snv 5
rs7382297
HLA-B
0.925 0.080 6 31279290 intron variant T/C;G snv 5
rs9652490
LINGO1
0.851 0.080 15 77671545 intron variant A/G snv 0.28 4
rs1036207
NDFIP1
1.000 0.080 5 142119476 intron variant A/G;T snv 3
rs10411936
EPS15L1
1.000 0.080 19 16437564 intron variant A/G snv 0.63 3
rs11621145
IGHA1
1.000 0.080 14 105706543 intron variant G/A snv 0.49 3
rs11949767
MXD3
1.000 0.080 5 177313243 upstream gene variant A/C;G snv 3
rs2640
EIF2AK1
0.925 0.080 7 6026819 missense variant T/C snv 9.0E-02 5.5E-02 3
rs371977426
P4HB
0.882 0.080 17 81859255 missense variant T/C snv 4.0E-06 7.0E-06 3
rs391745 0.925 0.080 X 97839482 intergenic variant C/G;T snv 3
rs4075958
RGS14
1.000 0.080 5 177357511 upstream gene variant G/A snv 0.21 3
rs4648356
TTC34
1.000 0.080 1 2792599 intron variant C/A snv 0.39 3
rs471979
NLRP5
0.925 0.080 19 56027610 missense variant G/C snv 0.13 9.7E-02 3
rs58124832
CACNA1H
0.925 0.080 16 1218376 missense variant G/A;T snv 5.5E-02 3
rs61731956
NR1H3 ; MADD
0.925 0.080 11 47268596 missense variant G/A snv 2.2E-04 2.6E-04 3
rs882300
LOC107985947
1.000 0.080 2 136218685 intergenic variant T/C;G snv 3