Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10158537
SDCCAG8
1 243324884 intron variant C/G;T snv 1
rs10159261
DNAJC16 ; AGMAT
1 15586492 non coding transcript exon variant G/T snv 0.30 1
rs10753629 1 163769110 downstream gene variant T/G snv 0.45 1
rs10857788
SYPL2
1 109469667 intron variant G/A snv 0.67 1
rs11166440 1 100342807 upstream gene variant A/G;T snv 1
rs1119066 1 186689080 regulatory region variant C/A snv 0.22 1
rs11211257
PIK3R3 ; P3R3URF-PIK3R3
1 46116261 intron variant A/G snv 0.11 1
rs11260709
CPLANE2
1 16231196 non coding transcript exon variant T/C snv 0.25 1
rs11261022
KLHDC7A
1 18481459 missense variant C/A snv 0.34 0.33 1
rs115276619
NIBAN1
1 184895998 intron variant T/A snv 1.1E-02 1
rs12024377
MFSD4A ; MFSD4A-AS1
1 205568730 upstream gene variant G/A snv 0.30 1
rs12061708
KLHDC7A
1 18483422 3 prime UTR variant G/A snv 0.26 1
rs12145670 1 56172718 non coding transcript exon variant T/C;G snv 1
rs12563200 1 23354137 TF binding site variant C/T snv 6.6E-02 1
rs12722725
PPM1J ; LOC105378910
1 112716059 non coding transcript exon variant T/C snv 8.9E-02 1
rs12736457
LOC105378910 ; PPM1J
1 112715671 upstream gene variant C/G snv 8.9E-02 1
rs17126268 1 102260843 intron variant T/C snv 7.3E-02 1
rs17413465 1 55253035 intron variant C/A;T snv 1
rs1757915 1 56150137 intron variant G/A snv 0.37 1
rs1763632 1 15985643 upstream gene variant T/C snv 0.90 1
rs1800674
COQ8A ; PSEN2
1 226898123 5 prime UTR variant A/G snv 0.54 1
rs1887252 1 82492188 intron variant G/C snv 0.69 1
rs1963869
SORT1
1 109358840 intron variant G/A;C snv 1
rs235485
PRRC2C
1 171559277 intron variant G/A snv 0.75 1
rs2577134 1 220050979 upstream gene variant C/T snv 0.63 1