Source: ALL

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: rs10766533
rs10766533
11 19203130 intron variant T/A snv 0.62
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2016 2016
dbSNP: rs10766533
rs10766533
11 19203130 intron variant T/A snv 0.62
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2016 2016
dbSNP: rs10766533
rs10766533
11 19203130 intron variant T/A snv 0.62
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2018 2018
dbSNP: rs10766533
rs10766533
11 19203130 intron variant T/A snv 0.62
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result)
0.700 1.000 1 2016 2016
dbSNP: rs1502987
rs1502987
11 19275793 intron variant T/C snv 0.26
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2019 2019
dbSNP: rs77055095
rs77055095
11 19199971 intron variant G/A snv 0.22
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2019 2019
dbSNP: rs77055095
rs77055095
11 19199971 intron variant G/A snv 0.22
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2019 2019
dbSNP: rs7951347
rs7951347
11 19198031 intron variant T/A;C snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs7951347
rs7951347
11 19198031 intron variant T/A;C snv
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs7951347
rs7951347
11 19198031 intron variant T/A;C snv
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs1648234
rs1648234
11 19308167 intron variant G/A snv 0.72
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.010 1.000 1 2011 2011