rs1135401746, GNB1

N. diseases: 7
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.
Dystonia
CUI: C0013421
Disease: Dystonia
97 0.827 0.400 1 1806512 missense variant C/G snv 0.700 0
Esotropia
CUI: C0014877
Disease: Esotropia
39 0.827 0.400 1 1806512 missense variant C/G snv 0.700 0
Generalized hypotonia
CUI: C1858120
Disease: Generalized hypotonia
164 0.827 0.400 1 1806512 missense variant C/G snv 0.700 0
Global developmental delay
CUI: C0557874
Disease: Global developmental delay
553 0.827 0.400 1 1806512 missense variant C/G snv 0.700 0
MENTAL RETARDATION, AUTOSOMAL DOMINANT 42
12 0.827 0.400 1 1806512 missense variant C/G snv 0.700 0
Precursor Cell Lymphoblastic Leukemia Lymphoma
168 0.827 0.400 1 1806512 missense variant C/G snv 0.700 0
Uranostaphyloschisis
CUI: C2981150
Disease: Uranostaphyloschisis
75 0.827 0.400 1 1806512 missense variant C/G snv 0.700 0