Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1744297
ASPG
14 104102135 intron variant T/C snv 0.86 12
rs2657879
GLS2 ; SPRYD4
1.000 0.080 12 56471554 missense variant A/G snv 0.17 0.15 9
rs12613336 2 210704675 regulatory region variant T/C snv 0.19 6
rs774211
RBMS2
12 56527155 intron variant T/C snv 0.12 4
rs7302925
SPRYD4 ; MIP
12 56467674 intron variant A/G snv 0.69 3