Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11039182
MADD
11 47325172 intron variant T/C snv 0.19 2
rs3816725
MADD
11 47284118 intron variant T/C;G snv 2
rs749067
MADD
11 47296606 intron variant T/C snv 0.26 2
rs753993
MADD
11 47328418 non coding transcript exon variant C/A snv 0.33 2
rs11039119
MIR6745 ; PACSIN3
11 47180373 intron variant G/A snv 0.38 0.33 2
rs7118178
MTCH2
11 47637583 intron variant G/A snv 0.20 2
rs11619319
PLUT
13 27913462 intron variant A/G snv 0.23 2
rs2979422
POLD2
7 44122756 intron variant T/C snv 0.20 2
rs11891554
PPM1G
2 27390750 intron variant G/A;T snv 7.1E-02 2
rs17712208
PROX1-AS1
1 213977102 intron variant T/A snv 2.1E-02 2
rs340878
PROX1-AS1 ; PROX1
1 213983706 intron variant G/C snv 0.63 2
rs3778321
RREB1
6 7250037 3 prime UTR variant G/A snv 0.11 2
rs3138708
SLC2A2
3 171009914 intron variant T/G snv 3.1E-02 2
rs5394
SLC2A2
3 171027104 intron variant G/A snv 0.15 2
rs2605627
SMCO4
11 93526349 intron variant A/G snv 0.79 2
rs2302593
SNRPD2 ; QPCTL
19 45693376 intron variant C/A;G snv 1.0E-04; 0.48 2
rs10500292
SYMPK
19 45824675 intron variant C/T snv 0.46 2
rs16980051
SYMPK
19 45842628 non coding transcript exon variant T/A;C snv 0.47 2
rs1124649
TMEM214
2 27037601 missense variant G/A snv 0.32 0.35 2
rs6072275
TOP1 ; PLCG1-AS1
20 41115265 intron variant G/A snv 0.13 2
rs3783347
WARS1
14 100372924 intron variant G/T snv 0.16 2
rs10278336
YKT6
7 44205764 intron variant A/C;G snv 2
rs10228456 1.000 0.080 7 15024301 intergenic variant C/T snv 0.54 3
rs12440695 15 62142957 regulatory region variant T/C snv 0.32 3
rs576674 1.000 0.080 13 32980164 intergenic variant G/A snv 0.69 3