Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs74570061
ARL9
1.000 0.080 4 56517605 intron variant T/C snv 3.9E-02 2
rs2657880
SPRYD4
12 56469986 3 prime UTR variant G/C snv 0.15 4
rs1998013 1 55492357 intron variant C/T snv 4.4E-03 1
rs12051548
TM4SF5
17 4779740 intron variant G/C snv 7.5E-02 1
rs4810479 1.000 0.040 20 45916409 upstream gene variant C/T snv 0.68 7
rs445925
APOC1
0.882 0.080 19 44912383 non coding transcript exon variant G/A;C snv 10
rs12040333
ST3GAL3
1.000 0.080 1 43848369 intron variant G/A;C snv 2
rs7442201
NSG1
1.000 0.080 4 4360022 intron variant A/C;G snv 2
rs77757620
STARD9
1.000 0.080 15 42661399 intron variant C/T snv 3.8E-02 2
rs751093906
SLC20A2
0.882 0.200 8 42472255 stop gained G/A;C snv 4.0E-06 8
rs115689251
LOC107985068
1.000 0.080 17 36032377 intergenic variant A/C snv 1.0E-02 2
rs7689240 1.000 0.080 4 35313869 intergenic variant A/G snv 0.21 2
rs7092929
LOC105376360 ; LINC02669
10 3496602 splice region variant A/C;T snv 1
rs8134546
LINC01426
1.000 0.080 21 34782568 intron variant T/C snv 8.7E-02 2
rs543554
FRY
1.000 0.080 13 32127501 intron variant A/G;T snv 2
rs448792
FRY
1.000 0.080 13 32103287 intron variant T/A;C snv 2
rs616082 18 31787677 intergenic variant C/A;T snv 1
rs8089491 18 31763291 upstream gene variant G/A snv 5.4E-02 1
rs10502575 18 31756628 downstream gene variant A/G snv 6.9E-02 1
rs6506900
LOC105372049
1.000 0.080 18 31226433 intergenic variant A/C;G snv 2
rs6506897 1.000 0.080 18 31215320 intergenic variant G/A snv 0.62 2
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs6606859
GABRG3
1.000 0.080 15 27032254 intron variant C/A;T snv 2
rs17214144
OSBPL3
1.000 0.080 7 24846128 intron variant T/C snv 0.20 2
rs91
LOC107986777
1.000 0.080 7 24409992 intron variant T/C snv 0.41 2