Details for Combination OLI1167

VARIANTS GNRHR:c.416G>A, p.Arg139His in Heterozygous form; GNRHR:c.30_31delinsAA, p.Asn10_Gln11delinsLysLys in Heterozygous form; CHD7:c.2053_2058dupGCAAAA, p.Lys683_Thr684insAlaLys in Heterozygous form
GENE COMBINATION CHD7; GNRHR
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 34198905
SCORES
FAMmanual
0

STAT
manualknowledgemeta
101

GENE
manualmanual harmonizedknowledgemeta
1101

VAR
manualknowledgemeta
000

FUN
manualmeta
00

FINAL
manualmeta
00


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