List of variants in gene TEX11 reported as pathogenic for spermatogenic failure, X-linked, 2

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_031276.3(TEX11):c.405C>T (p.Ala135=)	rs147088100	0.00245
NM_031276.3(TEX11):c.2047G>A (p.Ala683Thr)	rs140984555	0.00183
NM_031276.3(TEX11):c.466A>G (p.Met156Val)	rs143246552	0.00053
NC_000023.10:g.69954448_70045530del

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