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: rs62305038
rs62305038
4 99839008 intron variant C/T snv 0.33
Red cell distribution width determination
0.700 1.000 1 2019 2019
dbSNP: rs10883353
rs10883353
10 99496351 intergenic variant G/A snv 0.82
Red cell distribution width determination
0.700 1.000 1 2019 2019
dbSNP: rs2301889
rs2301889
7 99333482 intron variant A/G snv 0.13
Red cell distribution width determination
0.700 1.000 1 2019 2019
dbSNP: rs7182976
rs7182976
15 98753427 intron variant C/A;T snv
Red cell distribution width determination
0.700 1.000 1 2019 2019
dbSNP: rs1573891
rs1573891
15 98643259 downstream gene variant G/C snv 0.32
Red cell distribution width determination
0.700 1.000 1 2019 2019
dbSNP: rs12376113
rs12376113
9 97958017 regulatory region variant G/C snv 0.11
Red cell distribution width determination
0.700 1.000 1 2019 2019
dbSNP: rs2449511
rs2449511
8 97723714 intron variant A/G snv 9.2E-02
Red cell distribution width determination
0.700 1.000 1 2019 2019
dbSNP: rs2468024
rs2468024
8 97652425 intron variant G/A;C snv
Red cell distribution width determination
0.700 1.000 1 2017 2017
dbSNP: rs1155998
rs1155998
8 97639920 upstream gene variant C/A snv 0.22
Red cell distribution width determination
0.700 1.000 1 2016 2016
dbSNP: rs415895
rs415895
11 9748015 missense variant C/G snv 0.62 0.61
Red cell distribution width determination
0.700 1.000 1 2019 2019
dbSNP: rs3017756
rs3017756
11 95804194 intron variant G/A snv 0.35
Red cell distribution width determination
0.700 1.000 1 2019 2019
dbSNP: rs11021221
rs11021221
11 95575690 intron variant T/A;G snv
Red cell distribution width determination
0.700 1.000 1 2019 2019
dbSNP: rs632087
rs632087
11 95152471 intron variant C/T snv 0.59
Red cell distribution width determination
0.700 1.000 1 2019 2019
dbSNP: rs7078811
rs7078811
10 94596424 intron variant C/T snv 0.45
Red cell distribution width determination
0.700 1.000 1 2019 2019
dbSNP: rs9409793
rs9409793
9 94508873 intron variant C/A;G snv
Red cell distribution width determination
0.700 1.000 1 2017 2017
dbSNP: rs35219595
rs35219595
9 94506901 intron variant G/- delins 0.69
Red cell distribution width determination
0.700 1.000 1 2016 2016
dbSNP: rs67183237
rs67183237
10 94486139 intron variant C/T snv
Red cell distribution width determination
0.700 1.000 1 2017 2017
dbSNP: rs11187938
rs11187938
10 94423594 intron variant T/C snv 0.51
Red cell distribution width determination
0.700 1.000 1 2016 2016
dbSNP: rs10821339
rs10821339
9 94324185 intron variant G/A snv 0.28
Red cell distribution width determination
0.700 1.000 1 2019 2019
dbSNP: rs113792729
rs113792729
12 93326892 intron variant A/G snv 0.33
Red cell distribution width determination
0.700 1.000 1 2019 2019
dbSNP: rs739385
rs739385
7 93053295 regulatory region variant G/A;C snv
Red cell distribution width determination
0.700 1.000 2 2017 2019
dbSNP: rs2774952
rs2774952
1 92889689 intron variant A/C snv 0.68
Red cell distribution width determination
0.700 1.000 1 2019 2019
dbSNP: rs78084721
rs78084721
13 91366396 intergenic variant G/A snv 2.0E-02
Red cell distribution width determination
0.700 1.000 1 2019 2019
dbSNP: rs10801851
rs10801851
1 91281449 intron variant C/T snv 0.48
Red cell distribution width determination
0.700 1.000 1 2019 2019
dbSNP: rs17515485
rs17515485
15 91030274 intron variant T/G snv 6.4E-02
Red cell distribution width determination
0.700 1.000 1 2019 2019