"21-HYDROXYLASE POLYMORPHISM"[Disease/phenotype] AND "OMIM"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 12162	NM_000500.9(CYP21A2):c.17TGC[6] (p.Leu10dup)	CYP21A2, LOC106780800 +1 more	Microsatellite (inframe_insertion +1 more)	21-HYDROXYLASE POLYMORPHISM	GBenign
Select item 12154	NM_000500.9(CYP21A2):c.806G>C (p.Ser269Thr)	CYP21A2, LOC106780800 +1 more (S269T +2 more)	Single nucleotide variant (missense variant)	not specified +1 more	GBenign
Select item 12163	CYP21A2, TYR102ARG	CYP21A2	Single nucleotide variant	21-HYDROXYLASE POLYMORPHISM	GBenign

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