rs886039806, KIAA0586

N. diseases: 8
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.
Dextrocardia
CUI: C0011813
Disease: Dextrocardia
6 0.851 0.160 14 58467887 missense variant T/A;C;G snv 0.700 0
Dolichocephalic
CUI: C4697708
Disease: Dolichocephalic
1 0.851 0.160 14 58467887 missense variant T/A;C;G snv 0.700 0
Meckel-Gruber syndrome
CUI: C0265215
Disease: Meckel-Gruber syndrome
105 0.851 0.160 14 58467887 missense variant T/A;C;G snv 0.700 0
Narrow thorax
CUI: C0426790
Disease: Narrow thorax
18 0.851 0.160 14 58467887 missense variant T/A;C;G snv 0.700 0
Neonatal Death
CUI: C0410916
Disease: Neonatal Death
10 0.851 0.160 14 58467887 missense variant T/A;C;G snv 0.700 0
Occipital Encephalocele
CUI: C0014067
Disease: Occipital Encephalocele
9 0.851 0.160 14 58467887 missense variant T/A;C;G snv 0.700 0
Pericardial effusion
CUI: C0031039
Disease: Pericardial effusion
10 0.851 0.160 14 58467887 missense variant T/A;C;G snv 0.700 0
Polycystic Kidney Diseases
CUI: C0022680
Disease: Polycystic Kidney Diseases
54 0.851 0.160 14 58467887 missense variant T/A;C;G snv 0.700 0