rs876657400, SLC6A1

N. diseases: 2
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.
MYOCLONIC-ATONIC EPILEPSY
CUI: C4085238
Disease: MYOCLONIC-ATONIC EPILEPSY
16 0.925 0.080 3 11025812 missense variant G/A snv 0.800 0
Angelman Syndrome
CUI: C0162635
Disease: Angelman Syndrome
135 0.925 0.080 3 11025812 missense variant G/A snv 0.700 0