rs1801394, FASTKD3;MTRR

N. diseases: 101
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Vitiligo
CUI: C0042900
Disease: Vitiligo
249 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2019 2019
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding)
CUI: C1847835
Disease: VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding)
92 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2019 2019
Autism Spectrum Disorders
CUI: C1510586
Disease: Autism Spectrum Disorders
331 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2018 2018
Congenital Abnormality
CUI: C0000768
Disease: Congenital Abnormality
73 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2018 2018
Conotruncal defect
CUI: C1853238
Disease: Conotruncal defect
45 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2018 2018
Deformity
CUI: C0302142
Disease: Deformity
26 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2018 2018
Myasthenia Gravis
CUI: C0026896
Disease: Myasthenia Gravis
93 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2018 2018
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1 2018 2018
Skin lesion
CUI: C0037284
Disease: Skin lesion
52 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2018 2018
Meningioma
CUI: C0025286
Disease: Meningioma
43 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.020 1.000 2 2017 2017
Meningioma, benign, no ICD-O subtype
CUI: C1762616
Disease: Meningioma, benign, no ICD-O subtype
30 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.020 1.000 2 2017 2017
Ventricular Septal Defects
CUI: C0018818
Disease: Ventricular Septal Defects
87 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.020 1.000 2 2017 2019
Congenital heart disease
CUI: C0152021
Disease: Congenital heart disease
80 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2017 2017
Early childhood caries
CUI: C3714731
Disease: Early childhood caries
8 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2017 2017
Glioma
CUI: C0017638
Disease: Glioma
353 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2017 2017
Oligoasthenozoospermia
CUI: C3164407
Disease: Oligoasthenozoospermia
6 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2017 2017
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2016 2016
Ovarian Failure, Premature
CUI: C0085215
Disease: Ovarian Failure, Premature
115 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1 2016 2016
Premature Menopause
CUI: C0025322
Disease: Premature Menopause
90 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1 2016 2016
Stomatitis
CUI: C0038362
Disease: Stomatitis
22 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2016 2016
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.030 1.000 3 2015 2020
Dyslipidemias
CUI: C0242339
Disease: Dyslipidemias
184 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.020 1.000 2 2015 2020
Folic Acid Deficiency
CUI: C0016412
Disease: Folic Acid Deficiency
8 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.020 0.500 2 2015 2015
Azoospermia
CUI: C0004509
Disease: Azoospermia
70 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2015 2015
Color Blindness, Blue
CUI: C0155017
Disease: Color Blindness, Blue
12 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2015 2015