Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1000291485 1.000 0.107 2 43844563 stop gained C/G snp 1
rs1002088882 1.000 0.143 16 16219834 stop gained C/T snp 1
rs1002854345 10 93519809 splice donor variant T/A snp 1
rs1003869920 1.000 0.071 1 215674335 stop gained G/A snp 1
rs1006150317 1.000 0.107 19 12891875 stop gained G/T snp 1
rs1006246556 0.821 0.071 2 202556253 missense variant G/A,T snp 1
rs10065172 0.878 0.071 5 150848436 synonymous variant C/T snp 0.17 0.20 1
rs1006898944 19 36099453 stop gained C/T snp 1
rs1006994885 1.000 0.143 16 16150577 splice donor variant C/A,G snp 3.2E-05 1
rs1007345781 3 180616604 frameshift variant CTG/C in-del 8.7E-06 6.4E-05 1
rs1008240677 1.000 0.107 8 63086009 stop gained G/A snp 1
rs1008642 0.923 0.107 3 8733975 missense variant C/G,T snp 0.29 0.36 1
rs10090787 1.000 0.071 8 120798309 intron variant C/T snp 0.33 1
rs1009298200 1.000 0.071 16 5079077 synonymous variant C/T snp 1
rs1010666282
DMD
1.000 0.107 X 32411754 missense variant G/T snp 1
rs1010907740 1.000 8 144084471 missense variant T/C snp 1
rs1011196447 1.000 2 69354314 splice acceptor variant T/C snp 1
rs1011539285 1.000 15 44669391 missense variant A/G snp 6.5E-06 1
rs1013079991 1.000 0.107 11 62692475 splice acceptor variant T/C snp 1
rs1013147010 1.000 0.071 19 11105492 missense variant C/A snp 1
rs1013801316 1.000 0.143 11 89191418 missense variant G/A,T snp 1.2E-05 3.2E-05; 3.2E-05 1
rs1014317450 1.000 17 78997112 missense variant T/A snp 1.2E-05 1
rs1014959895 0.801 0.286 16 68329105 stop gained G/C,T snp 4.0E-06; 1.6E-05 15
rs1015798796 1.000 0.143 20 46725684 stop gained C/G snp 3.2E-05 1
rs1017946059
EVC
0.923 0.143 4 5731657 missense variant G/A snp 8.1E-06 2