List of variants in gene combination IDS, LOC106050102 reported as likely pathogenic by Myriad Genetics, Inc.

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_000202.8(IDS):c.631A>T (p.Lys211Ter)	rs2520863392
NM_000202.8(IDS):c.636del (p.Met212fs)	rs2520863301
NM_000202.8(IDS):c.671_672del (p.Gly224fs)	rs2520862741
NM_000202.8(IDS):c.695dup (p.Arg233fs)	rs2520862364
NM_000202.8(IDS):c.696_697del (p.Phe232fs)	rs2520862342
NM_000202.8(IDS):c.741_743delinsTA (p.Leu249fs)	rs2520852344

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