List of variants in gene RPL9 reported as uncertain significance by Ambry Genetics

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_000661.5(RPL9):c.564G>T (p.Gln188His)	rs748195496	0.00003
NM_000661.5(RPL9):c.265C>T (p.Arg89Cys)	rs200276230	0.00002
NM_000661.5(RPL9):c.167G>A (p.Arg56Gln)	rs571555380	0.00001
NM_000661.5(RPL9):c.335T>C (p.Val112Ala)	rs1019586152	0.00001
NM_000661.5(RPL9):c.568G>T (p.Ala190Ser)	rs1453715995	0.00001
NM_000661.5(RPL9):c.575A>G (p.Glu192Gly)	rs374515136	0.00001
NM_000661.5(RPL9):c.211C>T (p.Arg71Trp)
NM_000661.5(RPL9):c.503A>G (p.Lys168Arg)
NM_000661.5(RPL9):c.507C>G (p.Asn169Lys)

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