Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2068888 10 93079885 downstream gene variant G/A snv 0.42 5
rs66505542
BUD13
11 116752498 intron variant AA/-;A;AAA delins 5
rs78909033
RNPEPL1
2 240571486 intron variant G/A snv 9.2E-02 5
rs7896518
JMJD1C
10 63344740 intron variant A/G snv 0.38 5
rs11405616
NDFIP1
5 142130697 intron variant A/-;AA;AAA;AAAA delins 4
rs1354034
ARHGEF3
3 56815721 intron variant T/C snv 0.49 4
rs4432538
PLCB1 ; LOC105372521
20 8626746 intron variant G/A snv 0.52 4
rs56043070
GCSAML
1 247556467 splice donor variant G/A;T snv 5.2E-02; 4.1E-06 4
rs7529925
LINC01221
1 199038079 intron variant C/T snv 0.77 4
rs10058074
MIR3936HG
5 132350453 intron variant G/A snv 0.31 3
rs10466905 12 6393666 upstream gene variant G/A snv 0.21 3
rs1050316
MEF2D
1 156464911 3 prime UTR variant G/T snv 0.54 3
rs1059196
SEPT5-GP1BB ; GP1BB
22 19724571 3 prime UTR variant C/T snv 0.42 3
rs10914144
DNM3
1 171980610 intron variant T/C snv 0.78 3
rs10974808
RCL1
9 4840380 intron variant A/G snv 9.0E-02 3
rs11071720
TPM1-AS ; TPM1
15 63049797 intron variant T/C;G snv 3
rs117672662
ACTN1
14 68958750 intron variant T/C snv 7.4E-03 3
rs11789898
BRD3
9 134060541 intron variant G/T snv 0.14 3
rs12459847
MARK4
19 45247899 intron variant G/C snv 0.19 3
rs13300663
RCL1
9 4814948 intron variant G/A;C snv 3
rs139761834
CD36
7 80545045 intron variant T/C snv 2.8E-04 3
rs149290349
ZFP36L2
2 43224818 missense variant G/A;T snv 6.7E-02 3
rs17572109
ARPC2
2 218229211 non coding transcript exon variant G/A;T snv 3
rs34950321
IQGAP2
5 76668682 missense variant C/T snv 1.7E-02 1.6E-02 3
rs3804749
PDIA5
3 123114156 intron variant C/T snv 0.48 3