Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10055201
IL31RA
0.882 0.080 5 55865274 intron variant A/G snv 0.76 3
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs1027702 0.882 0.080 1 161743067 intergenic variant C/T snv 0.51 3
rs1039659576
MTR
0.689 0.520 1 236803473 missense variant A/G snv 21
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1045485
CASP8
0.637 0.480 2 201284866 missense variant G/A;C;T snv 4.0E-06; 9.0E-02 34
rs1047768
ERCC5 ; BIVM-ERCC5
0.695 0.320 13 102852167 synonymous variant T/C snv 0.52 0.59 20
rs1048108
SNHG31 ; BARD1
0.827 0.120 2 214809500 missense variant G/A snv 0.38 0.33 5
rs104893855
PHOX2B-AS1 ; PHOX2B
0.851 0.160 4 41747479 missense variant C/A snv 4
rs104893856
PHOX2B
0.827 0.080 4 41746162 missense variant C/T snv 6
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
rs104893878
SNCA ; SNCA-AS1
0.732 0.160 4 89835580 missense variant C/G snv 21
rs104893936
SNCB
0.851 0.120 5 176626472 missense variant C/G;T snv 5.6E-05 4
rs104893937
SNCB
0.851 0.120 5 176621218 missense variant G/T snv 1.7E-04 2.0E-04 4
rs104894103
APTX
0.807 0.280 9 32974495 stop gained C/G;T snv 4.0E-06; 1.6E-04 6
rs1051266
SLC19A1
0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 41
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1052536
LIG3
0.776 0.200 17 35004556 3 prime UTR variant C/T snv 0.42 0.36 10
rs1057519697
ALK
0.776 0.120 2 29220830 missense variant A/C snv 12
rs1057520018
STK11
0.807 0.080 19 1223124 missense variant T/C snv 6
rs1059111
NEFL
0.827 0.200 8 24952575 3 prime UTR variant T/A;G snv 5
rs10840002 0.882 0.080 11 8221479 downstream gene variant A/G snv 0.49 3
rs10895322
MMP20
0.851 0.120 11 102599525 intron variant A/G snv 9.4E-02 4
rs11037575
HSD17B12
0.882 0.080 11 43706780 intron variant T/C snv 0.36 4
rs110419
LOC105376536 ; LMO1
0.827 0.200 11 8231306 intron variant A/G snv 0.42 8