Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs74847330
ARHGAP15
2 143074030 intergenic variant A/G snv 8.8E-02 4
rs1059196
SEPT5-GP1BB ; GP1BB
22 19724571 3 prime UTR variant C/T snv 0.42 3
rs10886430
GRK5
10 119250744 intron variant A/G snv 8.8E-02 3
rs10914144
DNM3
1 171980610 intron variant T/C snv 0.78 3
rs11071720
TPM1-AS ; TPM1
15 63049797 intron variant T/C;G snv 3
rs11734132 4 6889792 intergenic variant G/C snv 0.17 3
rs117672662
ACTN1
14 68958750 intron variant T/C snv 7.4E-03 3
rs12445050
PLCG2
16 81837364 intron variant C/T snv 9.6E-02 3
rs139141690
CUX1
7 101856650 intron variant G/A snv 2.2E-03 3
rs17116384
ZBTB16
11 114110519 intron variant A/G snv 0.25 3
rs17396340
KIF1B
1 10226118 intron variant G/A;C snv 3
rs17572109
ARPC2
2 218229211 non coding transcript exon variant G/A;T snv 3
rs2157770
LOC100130548 ; BRD3
9 134056342 intron variant A/G snv 0.33 3
rs2287922
RASIP1
19 48728969 missense variant G/A snv 0.37 0.37 3
rs2393967
MIR1296 ; JMJD1C
10 63373396 intron variant A/C snv 0.23 3
rs34950321
IQGAP2
5 76668682 missense variant C/T snv 1.7E-02 1.6E-02 3
rs35150201
STMP1
7 135661514 upstream gene variant T/G snv 0.42 3
rs3804749
PDIA5
3 123114156 intron variant C/T snv 0.48 3
rs3842397
C18orf25
18 46265918 3 prime UTR variant TT/- del 0.43 3
rs41303899
TUBB1
20 59023753 missense variant G/A snv 8.7E-04 9.0E-04 3
rs41315846
GCSAML
1 247549001 intron variant T/C snv 0.44 0.52 3
rs4499344
PDCD5
19 32582525 intron variant G/A snv 0.46 3
rs4907622
GRTP1
13 113362571 intron variant G/C;T snv 3
rs553749201
CHRNE ; GP1BA
17 4933900 synonymous variant C/A snv 3
rs655029
EHD3
2 31254972 intron variant G/A snv 0.78 3