List of variants in gene SRY reported as uncertain significance 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: 13

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HGVS	dbSNP	gnomAD frequency
NM_003140.3(SRY):c.251G>C (p.Arg84Thr)	rs770778716	0.00001
NC_000024.9:g.(?_2654792)_(2655895_?)dup
NM_003140.3(SRY):c.226C>T (p.Arg76Cys)	rs2124486234
NM_003140.3(SRY):c.248C>A (p.Pro83His)	rs2051123246
NM_003140.3(SRY):c.253A>G (p.Met85Val)	rs2124486176
NM_003140.3(SRY):c.266A>C (p.Glu89Ala)	rs1556370554
NM_003140.3(SRY):c.272G>A (p.Ser91Asn)
NM_003140.3(SRY):c.31G>A (p.Val11Ile)
NM_003140.3(SRY):c.321G>T (p.Trp107Cys)	rs2051122910
NM_003140.3(SRY):c.472C>T (p.Gln158Ter)
NM_003140.3(SRY):c.556A>G (p.Ile186Val)
NM_003140.3(SRY):c.570del (p.Ser191fs)	rs1603308285
NM_003140.3(SRY):c.589C>A (p.Arg197Ser)	rs756606002

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