List of variants in gene RPS17 reported as uncertain significance for not provided

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001021.6(RPS17):c.14G>T (p.Arg5Leu)	rs2548306458
NM_001021.6(RPS17):c.152_154del (p.Ala51del)	rs1555451156
NM_001021.6(RPS17):c.159_160delinsCC (p.Val54Leu)

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