rs1801131, MTHFR

N. diseases: 93
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.
Conventional (Clear Cell) Renal Cell Carcinoma
222 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1 2019 2019
Deep Vein Thrombosis
CUI: C0149871
Disease: Deep Vein Thrombosis
93 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2019 2019
Glaucoma
CUI: C0017601
Disease: Glaucoma
198 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2019 2019
Ovarian Hyperstimulation Syndrome
CUI: C0085083
Disease: Ovarian Hyperstimulation Syndrome
24 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2019 2019
Polyp of large intestine
CUI: C0949059
Disease: Polyp of large intestine
32 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2019 2019
Renal Cell Carcinoma
CUI: C0007134
Disease: Renal Cell Carcinoma
288 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1 2019 2019
Thrombophilia
CUI: C0398623
Disease: Thrombophilia
43 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2019 2019
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.030 1.000 3 2018 2019
Hyperhomocysteinemia
CUI: C0598608
Disease: Hyperhomocysteinemia
45 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.020 1.000 2 2018 2018
Exfoliation Syndrome
CUI: C0206368
Disease: Exfoliation Syndrome
74 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1 2018 2018
Fanconi Anemia
CUI: C0015625
Disease: Fanconi Anemia
173 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1 2018 2018
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
194 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1 2018 2018
FRIEDREICH ATAXIA 1
CUI: C1856689
Disease: FRIEDREICH ATAXIA 1
24 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1 2018 2018
Psoriasis
CUI: C0033860
Disease: Psoriasis
705 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2018 2018
Vitamin B 12 Deficiency
CUI: C0042847
Disease: Vitamin B 12 Deficiency
11 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1 2018 2018
Adult Meningioma
CUI: C0278877
Disease: Adult Meningioma
30 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.020 1.000 2 2017 2017
Meningioma
CUI: C0025286
Disease: Meningioma
43 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.020 1.000 2 2017 2017
Meningioma, benign, no ICD-O subtype
30 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.020 1.000 2 2017 2017
Anterior encephalocele
CUI: C4024948
Disease: Anterior encephalocele
5 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2017 2017
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2017 2017
Gestational Trophoblastic Neoplasms
CUI: C1135868
Disease: Gestational Trophoblastic Neoplasms
7 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2017 2017
Glioma
CUI: C0017638
Disease: Glioma
353 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2017 2017
Hyperactive behavior
CUI: C0424295
Disease: Hyperactive behavior
112 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2017 2017
Impulsive Behavior
CUI: C0021125
Disease: Impulsive Behavior
69 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2017 2017
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.010 1.000 1 2017 2017