Disease: Platelet Component Distribution Width Measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12041331
PEAR1
0.776 0.200 1 156899922 intron variant G/A snv 0.19 11
rs150813342
GFI1B
9 132989126 synonymous variant C/T snv 4.1E-03 4.1E-03 9
rs6993770
ZFPM2 ; ZFPM2-AS1
0.925 0.080 8 105569300 intron variant A/T snv 0.31 9
rs11082304
CABLES1
18 23141009 intron variant G/C;T snv 6
rs11553699
TMEM120B ; RHOF
12 121779004 3 prime UTR variant A/G snv 9.4E-02 6
rs114694170
MEF2C ; MEF2C-AS1
1.000 0.040 5 88884379 non coding transcript exon variant T/C snv 3.6E-02 5
rs78909033
RNPEPL1
2 240571486 intron variant G/A snv 9.2E-02 5
rs4432538
PLCB1 ; LOC105372521
20 8626746 intron variant G/A snv 0.52 4
rs56043070
GCSAML
1 247556467 splice donor variant G/A;T snv 5.2E-02; 4.1E-06 4
rs1059196
SEPT5-GP1BB ; GP1BB
22 19724571 3 prime UTR variant C/T snv 0.42 3
rs11071720
TPM1-AS ; TPM1
15 63049797 intron variant T/C;G snv 3
rs117672662
ACTN1
14 68958750 intron variant T/C snv 7.4E-03 3
rs17572109
ARPC2
2 218229211 non coding transcript exon variant G/A;T snv 3
rs3804749
PDIA5
3 123114156 intron variant C/T snv 0.48 3
rs41303899
TUBB1
20 59023753 missense variant G/A snv 8.7E-04 9.0E-04 3
rs41315846
GCSAML
1 247549001 intron variant T/C snv 0.44 0.52 3
rs4907622
GRTP1
13 113362571 intron variant G/C;T snv 3
rs553749201
CHRNE ; GP1BA
17 4933900 synonymous variant C/A snv 3
rs655029
EHD3
2 31254972 intron variant G/A snv 0.78 3
rs7641175
TBC1D5
3 18269920 intron variant G/A snv 0.81 3
rs8073060
SLFN14 ; LOC107985032
17 35548243 missense variant T/A snv 0.32 0.34 3
rs1060431
SLC25A11
17 4937573 3 prime UTR variant G/A snv 0.13 2
rs10820606 9 96430637 intergenic variant A/C snv 0.23 2
rs11083766
BLOC1S3 ; EXOC3L2 ; MARK4
19 45212232 intron variant T/C snv 0.26 2
rs111941366
RHCE
1 25409878 intron variant C/T snv 0.30 2