rs1565286228, MYRF

N. diseases: 6
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.
Ambiguous Genitalia
CUI: C0266362
Disease: Ambiguous Genitalia
14 0.807 0.200 11 61766173 frameshift variant GCACCGGGCCCCCCATC/T delins 0.700 0
CARDIAC-UROGENITAL SYNDROME
CUI: C4748946
Disease: CARDIAC-UROGENITAL SYNDROME
7 0.807 0.200 11 61766173 frameshift variant GCACCGGGCCCCCCATC/T delins 0.700 0
Congenital diaphragmatic hernia
CUI: C0235833
Disease: Congenital diaphragmatic hernia
31 0.807 0.200 11 61766173 frameshift variant GCACCGGGCCCCCCATC/T delins 0.700 0
Horseshoe Kidney
CUI: C0221353
Disease: Horseshoe Kidney
3 0.807 0.200 11 61766173 frameshift variant GCACCGGGCCCCCCATC/T delins 0.700 0
Hydronephrosis
CUI: C0020295
Disease: Hydronephrosis
18 0.807 0.200 11 61766173 frameshift variant GCACCGGGCCCCCCATC/T delins 0.700 0
Penile hypospadias
CUI: C1691215
Disease: Penile hypospadias
83 0.807 0.200 11 61766173 frameshift variant GCACCGGGCCCCCCATC/T delins 0.700 0