Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs62160676
rs62160676
2 111410354 intron variant T/C;G snv
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 2 2016 2019
dbSNP: rs112744032
rs112744032
2 111521757 intron variant G/- delins
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2016 2016
dbSNP: rs143326447
rs143326447
0.925 0.080 2 111511155 intron variant T/C snv 0.11
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2019 2019
dbSNP: rs2009581
rs2009581
2 111050100 intron variant G/A snv 0.26
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2019 2019
dbSNP: rs2139376
rs2139376
2 111385836 intron variant T/C snv 0.44
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2019 2019
dbSNP: rs2334232
rs2334232
2 111371516 intron variant G/A snv 0.18
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2016 2016
dbSNP: rs4848370
rs4848370
2 111054088 intron variant C/T snv 0.25
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2016 2016
dbSNP: rs604126
rs604126
2 111185623 intron variant A/C;G;T snv
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2019 2019
dbSNP: rs616582
rs616582
2 111184418 intron variant T/C;G snv
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2016 2016