Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs398124647
CALM2
0.807 0.120 2 47161851 missense variant T/A;C snv 6
rs587782933
CACNA1C
0.827 0.200 12 2504526 missense variant G/A snv 5
rs4149000
SLCO1A2
0.882 0.080 12 21295063 non coding transcript exon variant C/T snv 0.11 5
rs587777598
ELOVL4
0.851 0.200 6 79921662 missense variant C/G;T snv 4
rs3512
FAN1 ; MTMR10
0.925 0.160 15 30942802 3 prime UTR variant G/C snv 0.27 4
rs1208917022
ATN1
1.000 0.040 12 6936663 missense variant A/G snv 3
rs786205753
CACNA1C
0.925 0.080 12 2593255 missense variant G/A snv 3
rs80315385
CACNA1C
0.882 0.200 12 2504932 missense variant G/A snv 3
rs192749597
CACNA1C ; CACNA1C-AS1
0.882 0.080 12 2679712 missense variant C/T snv 9.2E-04 3.5E-03 3
rs730880082
DSP
0.882 0.120 6 7576986 stop gained C/G;T snv 3
rs1458500258
RYR2
0.925 0.080 1 237388098 missense variant G/T snv 7.0E-06 3
rs11720524
SCN5A
0.882 0.080 3 38633921 intron variant C/G;T snv 0.34 3
rs11567847
TEAD1
0.925 0.120 11 12937202 missense variant T/C snv 3
rs17779747 1.000 0.040 17 70498851 regulatory region variant G/T snv 0.24 2
rs3730070
ADCY6
0.925 0.120 12 48775065 intron variant G/C snv 0.13 0.23 2
rs3734960
DPP6
0.925 0.240 7 154892443 missense variant T/C snv 0.33 0.36 2
rs104894393
FGF14
0.925 0.120 13 101726785 missense variant A/G snv 2
rs1805323
PMS2
0.925 0.160 7 5987311 missense variant G/A;T snv 4.0E-06; 8.0E-02 2
rs606231451
TMEM240
0.925 0.120 1 1535372 missense variant G/A snv 2
rs386418 1.000 0.040 Y 3213255 intergenic variant G/C snv 1
rs7208480 1.000 0.040 17 15770470 non coding transcript exon variant C/T snv 0.28 1
rs876188 1.000 0.040 14 98012267 intergenic variant G/A snv 0.66 1
rs149767043
C20orf194
1.000 0.040 20 3343726 missense variant G/C snv 4.0E-06 7.0E-06 1
rs3864180
GPC5
1.000 0.040 13 91784234 intron variant A/G;T snv 1
rs138694505
SEMA3A
1.000 0.040 7 84007493 missense variant T/C snv 3.4E-03 6.6E-03 1