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: rs1001494
rs1001494
1 112567997 intron variant T/C snv 0.50
Platelet mean volume determination (procedure)
0.700 1.000 1 2016 2016
dbSNP: rs10857961
rs10857961
1 112539531 intron variant C/A;T snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs12045227
rs12045227
1 112585590 intron variant G/A snv 0.19
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 1 2018 2018
dbSNP: rs12118370
rs12118370
1 112605645 intron variant A/G snv 0.24
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption
Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs12118370
rs12118370
1 112605645 intron variant A/G snv 0.24
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 1 2018 2018
dbSNP: rs12118370
rs12118370
1 112605645 intron variant A/G snv 0.24
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure
0.700 1.000 1 2018 2018
dbSNP: rs12730156
rs12730156
1 112587437 intron variant A/G snv 0.12
RDW - Red blood cell distribution width result
0.700 1.000 1 2019 2019
dbSNP: rs12730156
rs12730156
1 112587437 intron variant A/G snv 0.12
Red cell distribution width determination
0.700 1.000 1 2019 2019
dbSNP: rs2273368
rs2273368
1 112521149 3 prime UTR variant C/G;T snv
CUI: C0424621
Disease: Body Fat Distribution
Body Fat Distribution
0.700 1.000 1 2019 2019
dbSNP: rs6658555
rs6658555
1 112555912 missense variant C/T snv 0.19 0.20
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 1 2016 2016
dbSNP: rs6658555
rs6658555
1 112555912 missense variant C/T snv 0.19 0.20
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure
0.700 1.000 1 2016 2016
dbSNP: rs7546094
rs7546094
1 112611778 intron variant C/T snv 0.50
Platelet Component Distribution Width Measurement
0.700 1.000 1 2016 2016