Disease: Red cell distribution width determination
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17534202 1.000 0.120 1 203312047 downstream gene variant G/C snv 0.40 6
rs2492301
LINC01137 ; ZC3H12A
1 37473572 intron variant T/C snv 0.53 4
rs3768321
PABPC4 ; PABPC4-AS1
1.000 0.080 1 39570256 intron variant G/T snv 0.14 5
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26 12
rs12712870
LOC105374567
2 42934040 intergenic variant A/G snv 0.57 3
rs13007705
ERFE
2 238160555 intron variant C/T snv 0.46 3
rs17302154 2 196183605 intergenic variant A/C snv 9.8E-02 3
rs183034862
LOC102724081 ; CERS6
2 168457008 intron variant C/T snv 1.8E-02 3
rs2009581
ACOXL ; MIR4435-2HG
2 111050100 intron variant G/A snv 0.26 3
rs55709272
IL1RN
2 113109711 intron variant T/A;C snv 5
rs6730558
LOC105373411
2 8616053 intron variant C/T snv 0.47 5
rs78694551
GPR75-ASB3 ; ASB3
2 53751676 intron variant A/G;T snv 3
rs920112
CDCA7
2 173354407 intron variant G/A snv 1.0E-01 5
rs116577908
PLCL2
3 17056907 intron variant A/G snv 7.1E-03 4
rs1505307
THRB
3 24301839 intron variant T/C snv 0.60 6
rs8177318
INHCAP ; TF
3 133748533 missense variant T/A snv 1.6E-04 2.9E-04 5
rs9850274 3 196195556 downstream gene variant A/G snv 0.76 3
rs17076726
CPEB4
5 173936886 intron variant C/T snv 0.43 3
rs35188965
SLC12A7
5 1104823 intron variant C/G;T snv 12
rs3756668
PIK3R1
0.925 0.160 5 68300260 3 prime UTR variant G/A;C snv 3
rs112233623
CCND3
6 41957260 intron variant C/T snv 7.0E-03 5
rs116272812
CARMIL1
6 25452555 3 prime UTR variant T/C snv 8.1E-02 3
rs11756659 6 25933704 upstream gene variant A/G;T snv 4
rs144861591 6 26072764 intergenic variant C/T snv 3.8E-02 6
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 16