List of variants in gene AMHR2 reported as likely pathogenic for indeterminate sex and/or pseudohermaphroditism

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_020547.3(AMHR2):c.1483C>T (p.Arg495Trp)	rs749715622	0.00001
NM_020547.3(AMHR2):c.160C>T (p.Arg54Cys)
NM_020547.3(AMHR2):c.43del (p.Val15fs)	rs2136938115
NM_020547.3(AMHR2):c.514C>T (p.Arg172Ter)

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