ClinVar Miner

List of variants in gene STS reported as likely benign for X-linked recessive disease

Included ClinVar conditions (16):

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001320752.2(STS):c.383-16C>T	rs56055086	0.00332
NM_001320752.2(STS):c.259+8_259+10del	rs773065157

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