Source: GWASCAT

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: rs2291428
rs2291428
MARCHF8 ; LOC105378286
10 45463408 missense variant G/C snv 0.24 0.23
CUI: C0242216
Disease: Biliary calculi
Biliary calculi 		0.700 1.000 1 2018 2018
dbSNP: rs34285816
rs34285816
MARCHF8 ; LOC105378286
10 45481403 intron variant G/A snv 6.3E-02
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs34897497
rs34897497
MARCHF8
10 45529229 intron variant A/G snv 6.2E-02
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2016 2016
dbSNP: rs35993099
rs35993099
MARCHF8 ; LOC105378286
10 45511519 intron variant T/A snv 6.2E-02
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs35993099
rs35993099
MARCHF8 ; LOC105378286
10 45511519 intron variant T/A snv 6.2E-02
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2016 2016
dbSNP: rs3802548
rs3802548
MARCHF8
10 45457297 3 prime UTR variant T/A;C snv
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2019 2019
dbSNP: rs3802548
rs3802548
MARCHF8
10 45457297 3 prime UTR variant T/A;C snv
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2019 2019
dbSNP: rs71494799
rs71494799
MARCHF8 ; LOC105378286
10 45507408 intron variant T/C snv 4.9E-02
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019
dbSNP: rs77677521
rs77677521
MARCHF8
10 45457448 3 prime UTR variant C/G snv 1.3E-02
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2016 2016
dbSNP: rs77677521
rs77677521
MARCHF8
10 45457448 3 prime UTR variant C/G snv 1.3E-02
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2017 2017
dbSNP: rs77677521
rs77677521
MARCHF8
10 45457448 3 prime UTR variant C/G snv 1.3E-02
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2017 2017
dbSNP: rs77677521
rs77677521
MARCHF8
10 45457448 3 prime UTR variant C/G snv 1.3E-02
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2016 2016
dbSNP: rs7908745
rs7908745
MARCHF8
10 45458319 missense variant A/G snv 0.31 0.33
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs963029
rs963029
MARCHF8 ; LOC105378286
10 45467939 intron variant C/T snv 0.24
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2017 2017