List of variants in gene combination AR, LOC109504725 reported as pathogenic by Clinical Molecular Genetics Laboratory, Johns Hopkins All Children's Hospital

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000044.6(AR):c.214C>T (p.Gln72Ter)	rs1555969512
NM_000044.6(AR):c.217C>T (p.Gln73Ter)	rs1199988820
NM_000044.6(AR):c.220C>T (p.Gln74Ter)	rs886041129

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