Disease: Red cell distribution width determination
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs77677521
MARCHF8
10 45457448 3 prime UTR variant C/G snv 1.3E-02 4
rs781191470
AXIN1
16 307744 intron variant G/A snv 3.1E-04 4
rs8013143
PSMB5
14 23025068 intron variant A/G snv 0.43 4
rs112233623
CCND3
6 41957260 intron variant C/T snv 7.0E-03 5
rs2272783
FECH
1.000 18 57571588 synonymous variant A/G snv 0.12 6.3E-02 5
rs2857078
SLC4A1
17 44252803 intron variant A/C snv 0.62 5
rs3756668
PIK3R1
0.925 0.160 5 68300260 3 prime UTR variant G/A;C snv 5
rs3768321
PABPC4 ; PABPC4-AS1
1.000 0.080 1 39570256 intron variant G/T snv 0.14 5
rs55709272
IL1RN
2 113109711 intron variant T/A;C snv 5
rs6014993 20 57416581 regulatory region variant A/G snv 0.58 5
rs6730558
LOC105373411
2 8616053 intron variant C/T snv 0.47 5
rs920112
CDCA7
2 173354407 intron variant G/A snv 1.0E-01 5
rs144861591 6 26072764 intergenic variant C/T snv 3.8E-02 6
rs35158985
CDH1
0.882 0.080 16 68762843 intron variant A/G snv 0.38 6
rs10758656
RCL1
9 4852599 intron variant A/G snv 0.19 7
rs1505307
THRB
3 24301839 intron variant T/C snv 0.60 7
rs17534202 1.000 0.120 1 203312047 downstream gene variant G/C snv 0.40 7
rs7225002
KANSL1
0.925 0.080 17 46111701 intron variant A/G snv 0.39 7
rs737092 20 57415349 regulatory region variant T/C snv 0.58 7
rs8177318
INHCAP ; TF
3 133748533 missense variant T/A snv 1.6E-04 2.9E-04 7
rs9349205
CCND3
6 41957421 intron variant G/A;C snv 7
rs17476364
HK1
10 69334748 intron variant T/C snv 6.4E-02 8
rs9487023
CCDC162P
6 109268801 intron variant A/G snv 0.40 8
rs35979828
NFE2
12 54292096 intron variant C/T snv 5.0E-02 9
rs2277339
HSD17B6 ; PRIM1
12 56752285 missense variant T/G snv 0.12 0.14 10