Disease: Platelet Count measurement
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs10876550
COPZ1
12 54318524 intron variant G/A snv 0.68 2
rs10914144
DNM3
1 171980610 intron variant T/C snv 0.78 2
rs10940072
MAST4
5 66620956 intron variant G/A snv 0.37 2
rs11071720
TPM1-AS ; TPM1
15 63049797 intron variant T/C;G snv 3
rs11082304
CABLES1
18 23141009 intron variant G/C;T snv 5
rs112505971
ANKRD26
10 27068541 intron variant A/C;G snv 13
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
rs11604127
ODF3 ; BET1L
11 196944 5 prime UTR variant C/T snv 0.17 2
rs117672662
ACTN1
14 68958750 intron variant T/C snv 7.4E-03 3
rs12096438
LDLRAP1
1 25562931 non coding transcript exon variant C/A;T snv 2
rs13042885 20 1944061 upstream gene variant C/A;T snv 2
rs13331259
FAM234A
16 249924 intron variant A/G snv 3.0E-02 14
rs1354034
ARHGEF3
3 56815721 intron variant T/C snv 0.49 4
rs143558304
TPM4
19 16102887 3 prime UTR variant -/A delins 4.6E-02 2
rs150813342
GFI1B
9 132989126 synonymous variant C/T snv 4.1E-03 4.1E-03 9
rs151233
CLN3 ; APOBR
16 28495107 synonymous variant C/T snv 0.14 0.13 2
rs1716505
RASSF3 ; LOC105369804
12 64611299 intron variant C/G snv 0.34 2
rs17572109
ARPC2
2 218229211 non coding transcript exon variant G/A;T snv 3
rs17758695
BCL2
18 63253621 intron variant C/T snv 2.1E-02 10
rs17825630
ARHGEF3
3 56916027 intron variant G/A snv 0.12 2
rs2015599
LOC100506606 ; FAR2
12 29282547 non coding transcript exon variant G/A snv 0.51 2