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
rs9972293
C15orf41
15 36578054 upstream gene variant T/C snv 0.37 3
rs855791
TMPRSS6
0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 38
rs6000550
TMPRSS6
22 37067410 intron variant C/G;T snv 0.21 4
rs35893164
PIM1
6 37175357 3 prime UTR variant A/G snv 6.5E-03 4
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
rs6084653
SMOX
20 4176425 intron variant C/G;T snv 3
rs112233623
CCND3
6 41957260 intron variant C/T snv 7.0E-03 5
rs9349205
CCND3
6 41957421 intron variant G/A;C snv 7
rs9394841
CCND3
6 41959197 intron variant T/C snv 0.22 3
rs12712870
LOC105374567
2 42934040 intergenic variant A/G snv 0.57 3
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs2857078
SLC4A1
17 44252803 intron variant A/C snv 0.62 5
rs7789162
H2AZ2
7 44833301 intron variant T/C snv 0.48 3
rs741951
PTTG1IP
21 44849611 3 prime UTR variant G/A snv 0.14 4
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs62064595 17 45383008 regulatory region variant A/G snv 9.8E-02 3
rs77677521
MARCHF8
10 45457448 3 prime UTR variant C/G snv 1.3E-02 4
rs7225002
KANSL1
0.925 0.080 17 46111701 intron variant A/G snv 0.39 7
rs3740685
RAPSN
11 47447239 intron variant C/T snv 0.59 3
rs10758656
RCL1
9 4852599 intron variant A/G snv 0.19 7
rs595982
PPP1R15A
19 48874988 synonymous variant T/C snv 0.33 0.39 3
rs140522
ODF3B
0.851 0.160 22 50532837 upstream gene variant T/A;C snv 11
rs78694551
GPR75-ASB3 ; ASB3
2 53751676 intron variant A/G;T snv 3
rs6068729 20 53931121 intergenic variant C/T snv 0.19 3