Details for Combination OLI1682

VARIANTS INPPL1:c.3584G>T, p.Gly1195Val in Heterozygous form; GUCY2D:c.1720C>T, p.Arg574Cys in Heterozygous form; CDH23:c.7351A>G, p.Asn2451Asp in Heterozygous form; CDHR1:c.931C>A, p.Leu311Ile in Heterozygous form
GENE COMBINATION CDH23; CDHR1; GUCY2D; INPPL1
OLIGOGENIC EFFECT Unknown
ETHNICITY South American
OMIM IDS 617928; 148300
DISEASES Non-Syndromic genetic keratoconus
REFERENCES 37895187
SCORES
FAMmanual
0

STAT
manualknowledgemeta
000

GENE
manualmanual harmonizedknowledgemeta
1101

VAR
manualknowledgemeta
011

FUN
manualmeta
01

FINAL
manualmeta
00


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