rs1114167298, GRM7

N. diseases: 5
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.
Brain atrophy
CUI: C4551584
Disease: Brain atrophy
46 0.882 0.120 3 6861849 missense variant T/C snv 7.0E-06 0.700 0
Global developmental delay
CUI: C0557874
Disease: Global developmental delay
553 0.882 0.120 3 6861849 missense variant T/C snv 7.0E-06 0.700 0
Hypoplasia of corpus callosum
CUI: C0344482
Disease: Hypoplasia of corpus callosum
49 0.882 0.120 3 6861849 missense variant T/C snv 7.0E-06 0.700 0
Muscle hypotonia
CUI: C0026827
Disease: Muscle hypotonia
579 0.882 0.120 3 6861849 missense variant T/C snv 7.0E-06 0.700 0
Seizures
CUI: C0036572
Disease: Seizures
553 0.882 0.120 3 6861849 missense variant T/C snv 7.0E-06 0.700 0