ClinVar Miner

List of variants in gene combination CYP21A2, LOC106780800, LOC110631417 reported as benign for 46,XX disorder of sex development induced by androgens excess

Included ClinVar conditions (7):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 1
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NM_000500.9(CYP21A2):c.17_19TGC[6] (p.Leu10dup) rs61338903

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