Details for Combination OLI1605

VARIANTS HS6ST1:c.652C>T, p.Pro218Ser in Heterozygous form; CHD7:c.2966G>A, p.Cys989Tyr in Heterozygous form
GENE COMBINATION CHD7; HS6ST1
OLIGOGENIC EFFECT Unknown
ETHNICITY European/Caucasian
OMIM IDS 615269; 618841; 244200; 615267; 614880; 614837; 615270; 612702; 614838; 615271; 614840; 615266; 616030; 147950; 610628; 612370; 614858; 308700; 614897
DISEASES Kallmann syndrome
REFERENCES 29419413
SCORES
FAMmanual
0

STAT
manualknowledgemeta
101

GENE
manualmanual harmonizedknowledgemeta
1101

VAR
manualknowledgemeta
111

FUN
manualmeta
11

FINAL
manualmeta
00


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