List of variants in gene SRY reported as likely pathogenic for 46,XY complete gonadal dysgenesis

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_003140.3(SRY):c.192G>A (p.Met64Ile)	rs104894969
NM_003140.3(SRY):c.212C>A (p.Ser71Tyr)	rs2124486256
NM_003140.3(SRY):c.227G>T (p.Arg76Leu)	rs1057519627
NM_003140.3(SRY):c.263C>G (p.Ser88Ter)

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