SEPTIN11, septin 11, 55752

N. diseases: 23; N. variants: 2
Disease: AMYOTROPHY, HEREDITARY NEURALGIC ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs763296282
rs763296282 		1.000 0.040 4 77005693 missense variant C/T snv 2.8E-05 7.0E-06
CUI: C1834304
Disease: AMYOTROPHY, HEREDITARY NEURALGIC
AMYOTROPHY, HEREDITARY NEURALGIC 		Nervous System Diseases 0.010 1.000 1 2007 2007