Disease: Platelet Count measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6141
THPO
0.925 0.080 3 184372478 3 prime UTR variant C/G;T snv 4.0E-06; 0.56 4
rs41315846
GCSAML
1 247549001 intron variant T/C snv 0.44 0.52 3
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26 12
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 34
rs151233
CLN3 ; APOBR
16 28495107 synonymous variant C/T snv 0.14 0.13 2
rs6065
CHRNE ; GP1BA
0.851 0.280 17 4933086 missense variant C/T snv 9.8E-02 0.13 6
rs56043070
GCSAML
1 247556467 splice donor variant G/A;T snv 5.2E-02; 4.1E-06 4
rs34950321
IQGAP2
5 76668682 missense variant C/T snv 1.7E-02 1.6E-02 3
rs150813342
GFI1B
9 132989126 synonymous variant C/T snv 4.1E-03 4.1E-03 9
rs334
HBB
0.724 0.240 11 5227002 missense variant T/A;C;G snv 3.5E-03 35
rs41303899
TUBB1
20 59023753 missense variant G/A snv 8.7E-04 9.0E-04 3
rs10220411
ACTN1-AS1
14 68985371 intron variant A/G snv 0.29 2
rs1059196
SEPT5-GP1BB ; GP1BB
22 19724571 3 prime UTR variant C/T snv 0.42 3
rs10761741
JMJD1C
1.000 0.040 10 63306426 intron variant G/T snv 0.38 4
rs10876550
COPZ1
12 54318524 intron variant G/A snv 0.68 2
rs10914144
DNM3
1 171980610 intron variant T/C snv 0.78 3
rs10940072
MAST4
5 66620956 intron variant G/A snv 0.37 2
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 12
rs11071720
TPM1-AS ; TPM1
15 63049797 intron variant T/C;G snv 3
rs11082304
CABLES1
18 23141009 intron variant G/C;T snv 6
rs112505971
ANKRD26
10 27068541 intron variant A/C;G snv 13
rs114694170
MEF2C ; MEF2C-AS1
1.000 0.040 5 88884379 non coding transcript exon variant T/C snv 3.6E-02 5
rs11471957
TUBB1
20 59023277 intron variant -/AA ins 2
rs11553699
TMEM120B ; RHOF
12 121779004 3 prime UTR variant A/G snv 9.4E-02 6
rs11602954
BET1L
11 202856 intron variant G/A snv 0.17 2