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
rs1958078
SMOC1
14 69888141 intron variant A/C;G snv 4
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 15
rs2009581
ACOXL ; MIR4435-2HG
2 111050100 intron variant G/A snv 0.26 3
rs2272783
FECH
1.000 18 57571588 synonymous variant A/G snv 0.12 6.3E-02 5
rs2277339
HSD17B6 ; PRIM1
12 56752285 missense variant T/G snv 0.12 0.14 10
rs2468024
MTDH
8 97652425 intron variant G/A;C snv 3
rs2492301
LINC01137 ; ZC3H12A
1 37473572 intron variant T/C snv 0.53 4
rs2537594 7 17774912 intergenic variant G/A snv 0.58 3
rs2834259
ITSN1
21 33760786 intron variant C/T snv 0.30 3
rs2857078
SLC4A1
17 44252803 intron variant A/C snv 0.62 5
rs28601761 1.000 0.040 8 125487789 intron variant C/G snv 0.37 13
rs3208787
NPLOC4
17 81558634 3 prime UTR variant A/G snv 0.24 4
rs34536858 19 35459272 intergenic variant A/G snv 0.33 3
rs35158985
CDH1
0.882 0.080 16 68762843 intron variant A/G snv 0.38 6
rs35188965
SLC12A7
5 1104823 intron variant C/G;T snv 12
rs35893164
PIM1
6 37175357 3 prime UTR variant A/G snv 6.5E-03 4
rs35979828
NFE2
12 54292096 intron variant C/T snv 5.0E-02 9
rs368865
ATP11A
13 112825506 missense variant A/C;G;T snv 0.76; 4.0E-06 4
rs3740685
RAPSN
11 47447239 intron variant C/T snv 0.59 3
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
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26 12
rs4332427 10 24569461 intergenic variant A/G snv 0.21 3
rs532591337 19 12459271 intron variant G/A snv 4.9E-05 4
rs55709272
IL1RN
2 113109711 intron variant T/A;C snv 5