rs1057523354, COL4A1

N. diseases: 13
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.
Angioedema
CUI: C0002994
Disease: Angioedema
8 0.763 0.480 13 110179387 missense variant C/A snv 0.700 0
Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps
CUI: C2673195
Disease: Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps
18 0.763 0.480 13 110179387 missense variant C/A snv 0.700 0
Arthritis
CUI: C0003864
Disease: Arthritis
69 0.763 0.480 13 110179387 missense variant C/A snv 0.700 0
Depressive disorder
CUI: C0011581
Disease: Depressive disorder
297 0.763 0.480 13 110179387 missense variant C/A snv 0.700 0
Fatigue
CUI: C0015672
Disease: Fatigue
67 0.763 0.480 13 110179387 missense variant C/A snv 0.700 0
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.763 0.480 13 110179387 missense variant C/A snv 0.700 0
Hypothyroidism
CUI: C0020676
Disease: Hypothyroidism
283 0.763 0.480 13 110179387 missense variant C/A snv 0.700 0
Leukodystrophy
CUI: C0023520
Disease: Leukodystrophy
27 0.763 0.480 13 110179387 missense variant C/A snv 0.700 0
Low Vision
CUI: C0042798
Disease: Low Vision
51 0.763 0.480 13 110179387 missense variant C/A snv 0.700 0
Porencephaly, Type 1, Autosomal Dominant
CUI: C4551998
Disease: Porencephaly, Type 1, Autosomal Dominant
15 0.763 0.480 13 110179387 missense variant C/A snv 0.700 0
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.763 0.480 13 110179387 missense variant C/A snv 0.700 0
Sleep Apnea Syndromes
CUI: C0037315
Disease: Sleep Apnea Syndromes
18 0.763 0.480 13 110179387 missense variant C/A snv 0.700 0
Stroke-like episode
CUI: C1857287
Disease: Stroke-like episode
3 0.763 0.480 13 110179387 missense variant C/A snv 0.700 0