Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs16835904
RYR2
0.925 0.040 1 237833954 3 prime UTR variant C/T snv 0.17 2
rs2431689
MIR3142HG
0.882 0.040 5 160472115 intron variant G/A snv 0.17 3
rs2271338
ADGRL3
0.827 0.080 4 61996533 intron variant G/A snv 0.26 5
rs12594
RYR2
0.925 0.040 1 237833787 3 prime UTR variant A/G snv 0.28 2
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs1801275
IL4R
0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs7115578
MAML2
0.882 0.040 11 96266936 intron variant G/A snv 0.37 3
rs17522122
AKAP6
0.925 0.040 14 32833676 3 prime UTR variant G/T snv 0.41 5
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs4261436
AKAP6
0.925 0.040 14 32830276 3 prime UTR variant T/C snv 0.43 3
rs71305152
ZFPM2
0.882 0.040 8 105437494 intron variant -/TTTTCT delins 0.43 5
rs2297440
RTEL1 ; RTEL1-TNFRSF6B
0.763 0.080 20 63680946 intron variant T/C snv 0.81 10
rs6089953
RTEL1-TNFRSF6B ; RTEL1
0.882 0.080 20 63659655 intron variant A/G snv 0.82 3