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: rs2236659
rs2236659
1.000 0.040 11 123062473 non coding transcript exon variant A/G snv 0.11
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2019 2019
dbSNP: rs4802
rs4802
11 123057914 synonymous variant A/C;G snv 4.1E-06; 0.32
CUI: C0019693
Disease: HIV Infections
HIV Infections
Infections; Immune System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs4802
rs4802
11 123057914 synonymous variant A/C;G snv 4.1E-06; 0.32
CUI: C0373595
Disease: Creatinine clearance measurement
Creatinine clearance measurement
0.700 1.000 1 2015 2015
dbSNP: rs4936770
rs4936770
11 123058167 intron variant C/A;T snv
CUI: C0019693
Disease: HIV Infections
HIV Infections
Infections; Immune System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs4936770
rs4936770
11 123058167 intron variant C/A;T snv
CUI: C0373595
Disease: Creatinine clearance measurement
Creatinine clearance measurement
0.700 1.000 1 2015 2015
dbSNP: rs1136141
rs1136141
1.000 0.040 11 123062069 5 prime UTR variant G/A snv 0.14
CUI: C0338614
Disease: Psychotic episodes
Psychotic episodes
Mental Disorders 0.010 1.000 1 2014 2014
dbSNP: rs1366901063
rs1366901063
0.925 0.040 11 123060725 missense variant C/T snv 4.0E-06
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.010 1.000 1 2008 2008
dbSNP: rs1366901063
rs1366901063
0.925 0.040 11 123060725 missense variant C/T snv 4.0E-06
CUI: C4511452
Disease: Sporadic Parkinson disease
Sporadic Parkinson disease
Nervous System Diseases 0.010 1.000 1 2008 2008
dbSNP: rs2236659
rs2236659
1.000 0.040 11 123062473 non coding transcript exon variant A/G snv 0.11
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.010 1.000 1 2010 2010