Source: ALL
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: rs62130978
rs62130978
19 4429010 intron variant C/G;T snv 0.19
Red cell distribution width determination
0.700 1.000 2 2016 2017
dbSNP: rs62130978
rs62130978
19 4429010 intron variant C/G;T snv 0.19
RDW - Red blood cell distribution width result
0.700 1.000 2 2016 2017
dbSNP: rs11668886
rs11668886
19 4423422 intron variant C/T snv 0.18 0.17
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs12459919
rs12459919
19 4434506 intron variant C/G;T snv
Red cell distribution width determination
0.700 1.000 1 2019 2019
dbSNP: rs12459919
rs12459919
19 4434506 intron variant C/G;T snv
RDW - Red blood cell distribution width result
0.700 1.000 1 2019 2019
dbSNP: rs2267943
rs2267943
19 4413738 intron variant C/T snv 0.35
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs2293930
rs2293930
19 4444859 3 prime UTR variant C/T snv 0.36
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs243342
rs243342
19 4406163 intron variant G/A snv 0.53
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs243372
rs243372
19 4432976 intron variant G/A snv 0.50
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs243375
rs243375
19 4437092 intron variant C/G;T snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs243382
rs243382
19 4442532 intron variant T/C snv 0.59
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs243387
rs243387
19 4445159 3 prime UTR variant A/G;T snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs549220260
rs549220260
19 4426168 intron variant TTTTTTTT/-;TTTT;TTTTT;TTTTTT;TTTTTTT;TTTTTTTTT;TTTTTTTTTT;TTTTTTTTTTT delins
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result)
0.700 1.000 1 2016 2016
dbSNP: rs549220260
rs549220260
19 4426168 intron variant TTTTTTTT/-;TTTT;TTTTT;TTTTTT;TTTTTTT;TTTTTTTTT;TTTTTTTTTT;TTTTTTTTTTT delins
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2016 2016
dbSNP: rs62130981
rs62130981
19 4444446 intron variant C/T snv 0.28
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs932276
rs932276
19 4439528 intron variant G/A snv 0.36
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs9352
rs9352
19 4442339 missense variant C/G;T snv 0.58
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012