ClinVar Miner

List of variants reported as likely benign for 46,XX disorder of sex development induced by fetoplacental androgens excess by Illumina Clinical Services Laboratory,Illumina

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 7
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HGVS dbSNP
NM_000103.4(CYP19A1):c.*2632T>C
NM_000103.4(CYP19A1):c.*460G>C rs28757208
NM_000103.4(CYP19A1):c.*53C>T
NM_000103.4(CYP19A1):c.*543C>G
NM_000103.4(CYP19A1):c.115T>C (p.Trp39Arg) rs2236722
NM_000103.4(CYP19A1):c.383A>G (p.His128Arg)
NM_000103.4(CYP19A1):c.976C>T (p.Pro326Ser) rs368902124

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