Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10923398
rs10923398
1 117708553 regulatory region variant A/C snv 0.16
Red cell distribution width determination
0.700 1.000 3 2016 2019
dbSNP: rs17534202
rs17534202
1.000 0.120 1 203312047 downstream gene variant G/C snv 0.40
Red cell distribution width determination
0.700 1.000 3 2016 2019
dbSNP: rs183034862
rs183034862
2 168457008 intron variant C/T snv 1.8E-02
Red cell distribution width determination
0.700 1.000 3 2016 2019
dbSNP: rs2068229
rs2068229
3 141904462 intron variant A/G snv 0.35
Red cell distribution width determination
0.700 1.000 3 2016 2019
dbSNP: rs2075995
rs2075995
1 23520972 missense variant C/A snv 0.45 0.39
Red cell distribution width determination
0.700 1.000 3 2016 2019
dbSNP: rs3208787
rs3208787
17 81558634 3 prime UTR variant A/G snv 0.24
Red cell distribution width determination
0.700 1.000 3 2016 2019
dbSNP: rs35188965
rs35188965
5 1104823 intron variant C/G;T snv
Red cell distribution width determination
0.700 1.000 3 2016 2019
dbSNP: rs4332427
rs4332427
10 24569461 intergenic variant A/G snv 0.21
Red cell distribution width determination
0.700 1.000 3 2016 2019
dbSNP: rs4672497
rs4672497
2 62296430 TF binding site variant C/G;T snv
Red cell distribution width determination
0.700 1.000 3 2016 2019
dbSNP: rs6730558
rs6730558
2 8616053 intron variant C/T snv 0.47
Red cell distribution width determination
0.700 1.000 3 2016 2019
dbSNP: rs7148979
rs7148979
14 74080615 intron variant T/A snv 0.17
Red cell distribution width determination
0.700 1.000 3 2016 2019
dbSNP: rs73660574
rs73660574
9 132985025 intron variant G/A snv 5.3E-02
Red cell distribution width determination
0.700 1.000 3 2016 2019
dbSNP: rs7606173
rs7606173
1.000 0.080 2 60498316 intron variant G/C;T snv 0.39
Red cell distribution width determination
0.700 1.000 3 2016 2019
dbSNP: rs8013143
rs8013143
14 23025068 intron variant A/G snv 0.43
Red cell distribution width determination
0.700 1.000 3 2016 2019
dbSNP: rs8050500
rs8050500
16 31393250 upstream gene variant T/C snv 0.45
Red cell distribution width determination
0.700 1.000 3 2016 2019
dbSNP: rs8067342
rs8067342
17 21253548 upstream gene variant C/T snv 0.25
Red cell distribution width determination
0.700 1.000 3 2016 2019
dbSNP: rs9898189
rs9898189
17 82522640 intron variant C/A;G snv
Red cell distribution width determination
0.700 1.000 3 2016 2019
dbSNP: rs10210385
rs10210385
2 58770577 intron variant T/C snv 0.40
Red cell distribution width determination
0.700 1.000 2 2017 2019
dbSNP: rs10405535
rs10405535
19 32581179 upstream gene variant A/G;T snv
Red cell distribution width determination
0.700 1.000 2 2016 2017
dbSNP: rs1046321
rs1046321
17 35575265 3 prime UTR variant T/C snv 0.38
Red cell distribution width determination
0.700 1.000 2 2016 2017
dbSNP: rs1050828
rs1050828
0.790 0.200 X 154536002 missense variant C/T snv 9.1E-03 3.6E-02
Red cell distribution width determination
0.700 1.000 2 2013 2017
dbSNP: rs10988207
rs10988207
9 129104851 intron variant G/A;C;T snv
Red cell distribution width determination
0.700 1.000 2 2016 2017
dbSNP: rs11030967
rs11030967
11 4107890 intron variant C/T snv 0.51
Red cell distribution width determination
0.700 1.000 2 2016 2019
dbSNP: rs11133613
rs11133613
5 1074936 intron variant A/G snv 0.91
Red cell distribution width determination
0.700 1.000 2 2016 2017
dbSNP: rs111910553
rs111910553
5 1058272 intron variant G/A snv 1.1E-02
Red cell distribution width determination
0.700 1.000 2 2016 2017