Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 22
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 16
rs2890565
UTS2
0.732 0.440 1 7849677 missense variant C/T snv 8.7E-02 5.6E-02 15
rs228648
UTS2
0.776 0.360 1 7853370 missense variant G/A snv 0.51 0.52 13
rs5063
CLCN6 ; NPPA-AS1 ; NPPA
0.763 0.280 1 11847591 missense variant C/T snv 5.6E-02 5.3E-02 12
rs5065
NPPA ; CLCN6 ; NPPA-AS1
0.763 0.240 1 11846011 stop lost A/G snv 0.14 0.21 12
rs61672878
LMNA
0.776 0.200 1 156136094 missense variant G/A;T snv 11
rs4845625
IL6R
0.851 0.080 1 154449591 intron variant T/C snv 0.60 9
rs880315
CASZ1
0.925 0.120 1 10736809 intron variant T/C snv 0.32 9
rs28933093
LMNA
0.882 0.160 1 156130741 missense variant G/A snv 5
rs56793579
LMNA
0.851 0.240 1 156115102 missense variant C/G;T snv 5
rs58912633
LMNA
0.851 0.240 1 156130688 missense variant C/G;T snv 5
rs10465885
LOC102723321 ; GJA5
0.882 0.080 1 147760632 intron variant T/A;C snv 4
rs1046934
TSEN15
1.000 0.080 1 184054395 missense variant A/C;G;T snv 0.34; 4.0E-06 4
rs951366
NUCKS1
0.925 0.240 1 205716224 3 prime UTR variant T/C snv 0.34 4
rs121434558
GJA5 ; LOC102723321
0.882 0.120 1 147758977 missense variant G/A snv 3
rs121918603
RYR2
0.882 0.080 1 237639068 missense variant C/T snv 3
rs1253810269
ARID1A
0.882 0.080 1 26696971 missense variant G/A snv 7.0E-06 3
rs1273246817
RYR2
0.882 0.080 1 237784169 missense variant A/C snv 3
rs58672172
LMNA
0.882 0.160 1 156136251 missense variant C/T snv 1.2E-05 1.4E-05 3
rs6666258
KCNN3
0.882 0.080 1 154841792 intron variant G/C snv 0.30 3