List of variants in gene RPS5 reported as uncertain significance for not specified

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_001009.4(RPS5):c.274A>G (p.Ile92Val)	rs533747867	0.00001
NM_001009.4(RPS5):c.475C>A (p.Arg159Ser)	rs745755584	0.00001
NM_001009.4(RPS5):c.506T>C (p.Ile169Thr)	rs376539628	0.00001
NM_001009.4(RPS5):c.148C>T (p.Pro50Ser)
NM_001009.4(RPS5):c.32T>G (p.Val11Gly)	rs1200818651
NM_001009.4(RPS5):c.476G>A (p.Arg159His)	rs769796504

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