Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs863225401
MSH6 ; FBXO11
0.925 0.040 2 47799866 stop gained G/A snv 4
rs786205165
MTOR
0.882 0.120 1 11157173 missense variant C/A;T snv 4
rs1200941109
MYCN ; MYCNOS
0.882 0.040 2 15940679 frameshift variant C/-;CC delins 4
rs28357681
ND6 ; CYTB
0.851 0.040 MT 14798 missense variant T/C snv 4
rs1957106
NFKBIA
0.851 0.040 14 35404564 synonymous variant G/A snv 0.28 0.25 4
rs755794544
PDGFA
0.851 0.040 7 512435 missense variant T/C snv 4.0E-06 4
rs3851634
POLR3B
0.882 0.040 12 106419124 intron variant T/C snv 0.22 4
rs572480837
POU5F1 ; TCF19
0.851 0.040 6 31165582 missense variant T/A snv 5.0E-04 8.4E-05 4
rs200187877
PPARGC1A
0.851 0.040 4 23795829 missense variant C/T snv 8.0E-06 7.0E-06 4
rs12752552
RAVER2
0.882 0.040 1 64763616 intron variant T/C snv 0.13 4
rs8057643
RBFOX1
0.851 0.040 16 6910689 intron variant C/A;T snv 4
rs2562152
RHBDF1
0.882 0.040 16 73898 intron variant A/T snv 0.67 4
rs6062302
RTEL1 ; RTEL1-TNFRSF6B
0.882 0.040 20 63689615 synonymous variant T/C snv 0.74 0.81 4
rs2235573
SLC16A8
0.882 0.040 22 38081923 synonymous variant G/A snv 0.47 0.46 4
rs1340827343
TCF19 ; POU5F1
0.851 0.040 6 31165259 missense variant C/T snv 4
rs121912659
TP53
0.882 0.160 17 7673554 missense variant C/A;T snv 4.0E-06 7.0E-06 4
rs648044
ZBTB16 ; LOC101928875
0.882 0.040 11 114160077 non coding transcript exon variant A/G;T snv 4
rs17296479 0.851 0.040 5 81411157 non coding transcript exon variant T/A snv 9.4E-02 5
rs2440472
AMFR
0.827 0.080 16 56402912 intron variant A/G snv 0.61 5
rs373191257
AMFR
0.827 0.080 16 56363027 missense variant T/A snv 1.6E-05 7.0E-06 5
rs3092993
ATM ; C11orf65
0.827 0.040 11 108364388 intron variant C/A snv 0.11 5
rs373584770
CASP1
0.827 0.120 11 105030337 missense variant G/A snv 4.0E-06 7.0E-06 5
rs891835
CCDC26
0.851 0.120 8 129479506 intron variant T/G snv 0.17 5
rs11979158
EGFR
0.882 0.040 7 55091656 intron variant A/G;T snv 0.20 5
rs2234248
LOC105375056 ; TREM2
0.827 0.040 6 41163980 upstream gene variant A/G snv 2.2E-03 5