Disease: Red cell distribution width determination
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11756659 6 25933704 upstream gene variant A/G;T snv 4
rs140522
ODF3B
0.851 0.160 22 50532837 upstream gene variant T/A;C snv 10
rs144204502
TK1 ; AFMID
17 78187152 5 prime UTR variant C/G;T snv 1.2E-02 4
rs1958078
SMOC1
14 69888141 intron variant A/C;G snv 4
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 11
rs2468024
MTDH
8 97652425 intron variant G/A;C snv 3
rs35188965
SLC12A7
5 1104823 intron variant C/G;T snv 12
rs368865
ATP11A
13 112825506 missense variant A/C;G;T snv 0.76; 4.0E-06 4
rs3756668
PIK3R1
0.925 0.160 5 68300260 3 prime UTR variant G/A;C snv 3
rs55709272
IL1RN
2 113109711 intron variant T/A;C snv 5
rs6084653
SMOX
20 4176425 intron variant C/G;T snv 3
rs739385 7 93053295 regulatory region variant G/A;C snv 4
rs754205
IRS2
13 109759295 intron variant A/C;G snv 4
rs78694551
GPR75-ASB3 ; ASB3
2 53751676 intron variant A/G;T snv 3
rs79674254
AK9
6 109501078 intron variant C/A;T snv 3
rs855791
TMPRSS6
0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 17
rs9349205
CCND3
6 41957421 intron variant G/A;C snv 6
rs532591337 19 12459271 intron variant G/A snv 4.9E-05 4
rs8177318
INHCAP ; TF
3 133748533 missense variant T/A snv 1.6E-04 2.9E-04 5
rs781191470
AXIN1
16 307744 intron variant G/A snv 3.1E-04 4
rs35893164
PIM1
6 37175357 3 prime UTR variant A/G snv 6.5E-03 4
rs142529006
ZKSCAN1
7 100022093 intron variant T/A snv 6.9E-03 4
rs112233623
CCND3
6 41957260 intron variant C/T snv 7.0E-03 5
rs116577908
PLCL2
3 17056907 intron variant A/G snv 7.1E-03 4
rs148125759
UGCG
9 111901105 intron variant T/C snv 1.0E-02 4