Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11191454
LOC107984265 ; BORCS7-ASMT ; AS3MT
0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 5
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78 5
rs2524005
HLA-A
0.882 0.160 6 29931900 upstream gene variant G/A snv 0.18 5
rs17518584
CADM2
0.827 0.160 3 85555773 intron variant C/T snv 0.50 3
rs9378249 0.925 0.160 6 31359924 upstream gene variant T/A;G snv 3
rs10994336
ANK3
0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02 2
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 1
rs3130297 0.882 0.160 6 32231204 intergenic variant C/T snv 6.6E-02 1
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 7
rs1516725
ETV5 ; DGKG
0.925 0.120 3 186106215 intron variant T/C snv 0.86 7
rs9371601
SYNE1
0.790 0.120 6 152469438 intron variant G/T snv 0.46 6
rs28456
FADS1 ; FADS2
0.925 0.120 11 61822009 intron variant A/C;G snv 5
rs1906252 0.925 0.120 6 98102413 intron variant C/A;T snv 3
rs2251219
SMIM4 ; PBRM1
0.732 0.120 3 52550771 synonymous variant T/C;G snv 0.39; 4.0E-06 0.34 3
rs4523957
SMG6 ; SRR
0.790 0.120 17 2305605 intron variant G/T snv 0.54 2
rs1064395
NCAN
0.882 0.120 19 19250926 3 prime UTR variant G/A snv 0.24 1
rs121912734
ATP2A2
0.925 0.120 12 110339638 missense variant T/C snv 1
rs12290811
TENM4
0.882 0.120 11 79372576 intron variant T/A snv 0.18 1
rs12618769
MGAT4A
0.882 0.120 2 98623468 3 prime UTR variant C/T snv 0.18 1
rs17183814
SCN2A
0.827 0.120 2 165295879 splice acceptor variant G/A snv 8.4E-02 6.2E-02 1
rs2279574
DUSP6
0.827 0.120 12 89351700 missense variant C/A;T snv 0.52 1
rs6746896 0.851 0.120 2 96745212 intergenic variant A/G snv 0.26 1
rs78089757 0.882 0.120 10 125424260 intergenic variant G/A snv 9.9E-03 1
rs2710323
ITIH1
0.851 0.080 3 52781889 intron variant T/C snv 0.49 0.54 7
rs12576775
TENM4
0.827 0.080 11 79366149 intron variant A/G snv 0.15 6