Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2168889 4 74357994 intergenic variant A/G snv 4.7E-02 1
rs8089491 18 31763291 upstream gene variant G/A snv 5.4E-02 1
rs9973676
GPR55
1.000 0.080 2 230954091 intron variant G/A snv 5.8E-02 2
rs741013
PRICKLE2
3 64306961 intron variant A/T snv 6.0E-02 1
rs113805659
MAGI2
1.000 0.080 7 78663475 intron variant G/C snv 6.1E-02 2
rs17404667
PRICKLE2
3 64288876 intron variant C/G snv 6.2E-02 1
rs10502575 18 31756628 downstream gene variant A/G snv 6.9E-02 1
rs12051548
TM4SF5
17 4779740 intron variant G/C snv 7.5E-02 1
rs2306786
MYO1E
15 59195731 intron variant C/G snv 8.0E-02 1
rs59490629
PDSS2
1.000 0.080 6 107256268 intron variant G/A snv 8.5E-02 2
rs8134546
LINC01426
1.000 0.080 21 34782568 intron variant T/C snv 8.7E-02 2
rs12678919 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 10
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 15
rs9384331
LOC105378054
1.000 0.080 6 150279905 intergenic variant T/C snv 0.12 2
rs12507628 4 72779634 regulatory region variant G/A snv 0.13 1
rs2390582
LOC105378851
1 90478350 intergenic variant A/G snv 0.15 1
rs2657880
SPRYD4
12 56469986 3 prime UTR variant G/C snv 0.15 4
rs17214144
OSBPL3
1.000 0.080 7 24846128 intron variant T/C snv 0.20 2
rs217181
TXNL4B
16 72080103 intron variant C/T snv 0.20 6
rs7689240 1.000 0.080 4 35313869 intergenic variant A/G snv 0.21 2
rs1303
SERPINA1
0.925 0.040 14 94378506 missense variant T/G snv 0.28 0.22 4
rs7804216
ACTR3C
1.000 0.080 7 149941248 intergenic variant C/G snv 0.24 2
rs13175840 1.000 0.080 5 133861647 regulatory region variant A/G snv 0.25 2
rs749924
LINC01880
2 242084344 upstream gene variant C/T snv 0.25 1
rs634537
CDKN2B-AS1
0.851 0.080 9 22032153 intron variant T/G snv 0.28 6