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: rs196974
rs196974
X 28699359 intron variant G/A snv
CUI: C0008810
Disease: Circadian Rhythms
Circadian Rhythms
0.700 1.000 1 2016 2016
dbSNP: rs4829242
rs4829242
1.000 0.080 X 29613413 intron variant C/T snv 0.35
CUI: C0006287
Disease: Bronchopulmonary Dysplasia
Bronchopulmonary Dysplasia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases 0.700 1.000 1 2011 2011
dbSNP: rs6526874
rs6526874
1.000 0.080 X 29508403 intron variant T/A;C;G snv
CUI: C0006287
Disease: Bronchopulmonary Dysplasia
Bronchopulmonary Dysplasia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases 0.700 1.000 1 2011 2011
dbSNP: rs73456411
rs73456411
1.000 0.040 X 29719287 intron variant G/T snv 6.7E-02
CUI: C0042900
Disease: Vitiligo
Vitiligo
Skin and Connective Tissue Diseases 0.700 1.000 1 2016 2016
dbSNP: rs7890572
rs7890572
X 29622701 intron variant A/G snv 9.3E-02
CUI: C1168443
Disease: Pseudocholinesterase Measurement
Pseudocholinesterase Measurement
0.700 1.000 1 2010 2010
dbSNP: rs7890572
rs7890572
X 29622701 intron variant A/G snv 9.3E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2010 2010
dbSNP: rs7890572
rs7890572
X 29622701 intron variant A/G snv 9.3E-02
High density lipoprotein measurement
0.700 1.000 1 2010 2010
dbSNP: rs7890572
rs7890572
X 29622701 intron variant A/G snv 9.3E-02
CUI: C0455829
Disease: Waist Circumference
Waist Circumference
0.700 1.000 1 2010 2010
dbSNP: rs7890572
rs7890572
X 29622701 intron variant A/G snv 9.3E-02
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
Cardiovascular Diseases 0.700 1.000 1 2010 2010
dbSNP: rs7890572
rs7890572
X 29622701 intron variant A/G snv 9.3E-02
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2010 2010
dbSNP: rs878853146
rs878853146
1.000 0.200 X 29917576 frameshift variant TTGGGAAAGT/- delins
CUI: C0025362
Disease: Mental Retardation
Mental Retardation
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms 0.700 0
dbSNP: rs12007907
rs12007907
1.000 0.080 X 29465775 intron variant C/A snv 0.12
CUI: C0004096
Disease: Asthma
Asthma
Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2017 2017