Disease: Red Blood Cell Count measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4895441
LOC105378010
0.925 0.080 6 135105435 upstream gene variant A/G snv 0.21 10
rs9376092
LOC105378010
0.851 0.120 6 135106006 upstream gene variant C/A snv 0.24 10
rs35979828
NFE2
12 54292096 intron variant C/T snv 5.0E-02 9
rs17342717
SLC17A1
6 25821542 intron variant C/T snv 6.1E-02 8
rs17476364
HK1
10 69334748 intron variant T/C snv 6.4E-02 8
rs9487023
CCDC162P
6 109268801 intron variant A/G snv 0.40 8
rs10758656
RCL1
9 4852599 intron variant A/G snv 0.19 7
rs129128
H2BC4 ; H2AC6
6 26125114 intron variant C/T snv 0.91 7
rs1505307
THRB
3 24301839 intron variant T/C snv 0.60 7
rs17534202 1.000 0.120 1 203312047 downstream gene variant G/C snv 0.40 7
rs7203560
NPRL3
1.000 0.080 16 134391 intron variant T/G snv 2.0E-02 7
rs737092 20 57415349 regulatory region variant T/C snv 0.58 7
rs8887
PLIN4 ; HDGFL2
1.000 0.080 19 4502189 3 prime UTR variant T/C;G snv 0.51; 1.8E-05 7
rs9349205
CCND3
6 41957421 intron variant G/A;C snv 7
rs12216125 0.925 0.120 6 25997230 intron variant C/T snv 0.26 6
rs130624 22 37042611 regulatory region variant G/T snv 0.47 6
rs1434282
LINC01221
1 199041592 non coding transcript exon variant C/T snv 0.76 6
rs218237 4 54528005 intergenic variant C/T snv 0.18 6
rs228129
LOC112268295
22 37032558 upstream gene variant A/G snv 0.48 6
rs3887266
SLC17A3
0.925 0.120 6 25843518 intron variant C/T snv 8.9E-02 6
rs592423 6 139519556 intron variant A/C snv 0.50 6
rs9389268
HBS1L
1.000 0.080 6 135098493 intron variant A/G snv 0.24 6
rs112233623
CCND3
6 41957260 intron variant C/T snv 7.0E-03 5
rs113809617
TMEM203 ; NDOR1
9 137205865 missense variant C/G snv 0.13 0.12 5
rs11627485
FNTB ; CHURC1-FNTB ; MAX
14 65020976 intron variant T/C snv 0.36 5