rs1555859593, ATP1A3

N. diseases: 3
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.
Dysmorphic features
CUI: C0432072
Disease: Dysmorphic features
617 1.000 19 41970483 missense variant G/T snv 0.700 1.000 27 1988 2017
Multiple congenital anomalies
CUI: C0000772
Disease: Multiple congenital anomalies
350 1.000 19 41970483 missense variant G/T snv 0.700 1.000 27 1988 2017
Muscle hypotonia
CUI: C0026827
Disease: Muscle hypotonia
579 1.000 19 41970483 missense variant G/T snv 0.700 1.000 27 1988 2017