Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1000096
KLF3
4 38691214 intron variant C/T snv 0.39 1
rs10002111
LOC105377262
4 66949786 regulatory region variant A/G snv 0.82 1
rs1000940
RABEP1 ; NUP88
17 5379957 intron variant A/G snv 0.31 1
rs10016841
LOC105374514
4 20212158 intergenic variant T/C snv 0.16 1
rs10019997 4 136127444 intron variant C/T snv 0.47 1
rs1002226 11 17384070 downstream gene variant C/T snv 0.69 1
rs1003081 11 119043282 upstream gene variant C/T snv 0.38 1
rs10044136
MFAP3
5 154167248 intron variant G/C snv 0.54 1
rs10060123 5 126348218 intron variant C/A snv 0.22 1
rs10062657
LOC101929710 ; CAST
5 96532204 intron variant C/A snv 0.78 1
rs10063055
DIAPH1
5 141610541 intron variant C/T snv 0.22 1
rs10063334
MCC
5 113425177 intron variant T/C snv 0.31 1
rs1006353 13 27473132 regulatory region variant A/G snv 0.64 1
rs1006893
LOC400867
21 38931753 intron variant C/T snv 0.69 1
rs10091344 8 34274557 intron variant G/A;C snv 1
rs1009188
CRB1
1 197287960 intron variant T/C snv 0.22 1
rs10092723
LOC102724687
8 66282475 intergenic variant C/A snv 0.28 1
rs10099330
TSNARE1
8 142302333 intron variant A/G snv 0.53 1
rs10101364
LOC105379315
8 20777377 intergenic variant C/T snv 0.73 1
rs10102172 8 76326157 intergenic variant A/C;G snv 1
rs10104041
LOC101926977
8 94559374 intron variant G/A snv 0.33 1
rs1011407 2 60438633 intron variant A/G snv 7.7E-02 1
rs10116186
LOC107987081 ; GNAQ
9 77917458 intron variant A/C;G snv 1
rs10116857
BNC2
9 16595651 intron variant C/A;T snv 1
rs10132280 14 25458973 intergenic variant C/A snv 0.37 6