LNX2, ligand of numb-protein X 2, 222484

N. diseases: 5; N. variants: 4
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: rs76900683
rs76900683 		13 27583898 intron variant G/C snv 3.0E-02
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs76900683
rs76900683 		13 27583898 intron variant G/C snv 3.0E-02
CUI: C3828530
Disease: Platelet Component Distribution Width Measurement
Platelet Component Distribution Width Measurement 		0.700 1.000 1 2016 2016
dbSNP: rs1014369151
rs1014369151 		1.000 13 27623014 missense variant C/T snv
CUI: C3150983
Disease: TREACHER COLLINS SYNDROME 2
TREACHER COLLINS SYNDROME 2 		0.700 0
dbSNP: rs587777841
rs587777841 		1.000 13 27623011 missense variant C/G snv
CUI: C3150983
Disease: TREACHER COLLINS SYNDROME 2
TREACHER COLLINS SYNDROME 2 		0.700 0
dbSNP: rs767196650
rs767196650 		1.000 13 27622987 missense variant G/A snv 4.0E-06
CUI: C3150983
Disease: TREACHER COLLINS SYNDROME 2
TREACHER COLLINS SYNDROME 2 		0.700 0