Details for Combination OLI997

VARIANTS AR:c.1768G>C, p.Gly590Arg in Heterozygous form; BMP4:c.806G>A, p.Arg269Gln in Heterozygous form; POR:c.1876G>A, p.Gly626Ser in Heterozygous form; MAP3K1:c.2665G>C, p.Val889Leu in Heterozygous form
GENE COMBINATION AR; BMP4; MAP3K1; POR
OLIGOGENIC EFFECT Unknown
ETHNICITY East Asian
OMIM IDS N.A.
DISEASES 46,XY disorder of sex development; Androgen insensitivity syndrome
REFERENCES 33750429
SCORES
FAMmanual
0

STAT
manualknowledgemeta
000

GENE
manualmanual harmonizedknowledgemeta
0000

VAR
manualknowledgemeta
011

FUN
manualmeta
00

FINAL
manualmeta
00


Found any issues with the data on this page? Report this entry.