ANLN, anillin actin binding protein, 54443

N. diseases: 54; N. variants: 7
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: rs587777741
rs587777741 		0.925 7 36411062 missense variant C/T snv 1.7E-05 3.5E-05
CUI: C4014993
Disease: FOCAL SEGMENTAL GLOMERULOSCLEROSIS 8
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 8 		0.800 1.000 1 2014 2014
dbSNP: rs10224902
rs10224902 		7 36415868 synonymous variant T/C snv 0.13 0.12
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2019 2019
dbSNP: rs10224902
rs10224902 		7 36415868 synonymous variant T/C snv 0.13 0.12
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs3735398
rs3735398 		7 36406512 synonymous variant A/G snv 0.13 0.11
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2016 2016
dbSNP: rs55891665
rs55891665 		7 36406903 intron variant A/G snv 0.12
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019
dbSNP: rs1184529372
rs1184529372 		1.000 7 36419462 missense variant G/C;T snv 8.0E-06
CUI: C4014993
Disease: FOCAL SEGMENTAL GLOMERULOSCLEROSIS 8
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 8 		0.700 0
dbSNP: rs3735400
rs3735400 		7 36399100 missense variant C/G;T snv 0.13
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs3735400
rs3735400 		7 36399100 missense variant C/G;T snv 0.13
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs376778595
rs376778595 		1.000 0.040 7 36410522 missense variant G/A snv 4.2E-06
CUI: C0006272
Disease: Bronchiolitis Obliterans
Bronchiolitis Obliterans 		Respiratory Tract Diseases 0.010 1.000 1 2019 2019
dbSNP: rs587777741
rs587777741 		0.925 7 36411062 missense variant C/T snv 1.7E-05 3.5E-05
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		0.010 1.000 1 2014 2014