Disease: AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11987758
LOC105377781
0.851 0.080 8 2180583 regulatory region variant G/A snv 0.12 4
rs35714695
SARM1
0.827 0.080 17 28392769 intron variant G/A;T snv 0.12 5
rs9327881 0.851 0.080 5 103389394 intergenic variant G/A snv 0.13 4
rs1002442
ANK3
0.851 0.080 10 60043304 non coding transcript exon variant T/G snv 0.14 4
rs11590421
LOC105378658
0.851 0.080 1 38528443 intergenic variant G/A snv 0.15 4
rs9825420
ITGA9
0.851 0.080 3 37562521 intron variant T/G snv 0.18 4
rs730547
LOC105371742
0.851 0.080 17 34785087 intergenic variant C/T snv 0.20 4
rs7117082
OPCML
0.851 0.080 11 133522399 intron variant G/T snv 0.22 4
rs4234080
METTL21A
0.851 0.080 2 207624377 5 prime UTR variant C/A snv 0.19 0.23 4
rs9977018 0.851 0.080 21 41616809 intergenic variant T/G snv 0.24 4
rs6137726 0.851 0.080 20 22691782 intron variant C/A snv 0.25 4
rs1559473 0.851 0.080 2 222016799 intergenic variant T/G snv 0.25 4
rs2412208
CAMTA1
0.827 0.080 1 7032722 intron variant T/G snv 0.33 5
rs2457174
FSTL4
0.851 0.080 5 133843389 intergenic variant C/T snv 0.33 4
rs13100616
KCNMB2-AS1 ; KCNMB2
0.851 0.080 3 178681763 intron variant A/G snv 0.33 4
rs12608932
UNC13A
0.827 0.080 19 17641880 intron variant A/C snv 0.36 5
rs7830371
CLVS1
0.851 0.080 8 61143108 intron variant G/T snv 0.46 4
rs3852053
MASP1
0.851 0.080 3 187219412 3 prime UTR variant T/G snv 0.47 4
rs2685056
LOC107986108
0.851 0.080 3 104699729 intergenic variant G/A snv 0.50 4
rs1605070 0.851 0.080 3 51882999 intergenic variant C/A snv 0.60 4
rs12891047
ZFYVE26
0.851 0.080 14 67776358 intron variant C/A snv 0.62 4
rs2322978 0.851 0.080 11 127846245 intergenic variant A/G snv 0.74 4
rs4424056 0.851 0.080 6 91135689 intergenic variant T/G snv 0.76 4
rs616147
MOBP
0.827 0.080 3 39492990 intron variant A/G snv 0.76 5
rs2667100
INPP4B
0.851 0.080 4 142054920 intron variant A/G snv 0.81 4