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: rs970548
rs970548
MARCHF8
10 45517829 intron variant A/C;T snv
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 3 2013 2018
dbSNP: rs76934034
rs76934034
MARCHF8
1.000 0.080 10 45587537 intron variant T/C snv 5.7E-02
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.700 1.000 2 2014 2018
dbSNP: rs901683
rs901683
MARCHF8 ; LOC105378286
10 45470974 intron variant G/A snv 6.3E-02
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 2 2012 2017
dbSNP: rs970548
rs970548
MARCHF8
10 45517829 intron variant A/C;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.800 1.000 2 2013 2017
dbSNP: rs112297763
rs112297763
MARCHF8
10 45573988 intron variant T/C snv 6.5E-02
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2018 2018
dbSNP: rs11239537
rs11239537
MARCHF8 ; LOC105378286
10 45487060 intron variant T/C snv 0.33
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2016 2016
dbSNP: rs11239537
rs11239537
MARCHF8 ; LOC105378286
10 45487060 intron variant T/C snv 0.33
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2016 2016
dbSNP: rs11239541
rs11239541
MARCHF8 ; LOC105378286
10 45506418 intron variant C/T snv 0.33
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2019 2019
dbSNP: rs11239541
rs11239541
MARCHF8 ; LOC105378286
10 45506418 intron variant C/T snv 0.33
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs11239544
rs11239544
MARCHF8
10 45512085 intron variant C/G;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2015 2015
dbSNP: rs11239549
rs11239549
MARCHF8
10 45523383 intron variant A/G snv 0.26
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2018 2018
dbSNP: rs11239550
rs11239550
MARCHF8
10 45529281 intron variant A/G snv 0.31
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.800 1.000 1 2009 2009
dbSNP: rs11239550
rs11239550
MARCHF8
10 45529281 intron variant A/G snv 0.31
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2017 2017
dbSNP: rs149604913
rs149604913
MARCHF8 ; LOC105378286
10 45499558 intron variant T/C snv 1.4E-02
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2016 2016
dbSNP: rs149604913
rs149604913
MARCHF8 ; LOC105378286
10 45499558 intron variant T/C snv 1.4E-02
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2016 2016
dbSNP: rs17157825
rs17157825
MARCHF8 ; LOC105378286
10 45463228 synonymous variant G/A snv 3.7E-02 3.4E-02
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2018 2018
dbSNP: rs17157836
rs17157836
MARCHF8 ; LOC105378286
10 45468138 intron variant T/C snv 6.3E-02
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs2279434
rs2279434
MARCHF8
10 45459616 intron variant C/T snv 7.1E-02
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		0.700 1.000 1 2010 2010
dbSNP: rs2279434
rs2279434
MARCHF8
10 45459616 intron variant C/T snv 7.1E-02
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2010 2010
dbSNP: rs2279434
rs2279434
MARCHF8
10 45459616 intron variant C/T snv 7.1E-02
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2010 2010
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