List of variants in gene combination IQCG, RPL35A reported as likely benign by Fulgent Genetics, Fulgent 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000996.4(RPL35A):c.21C>T (p.Ser7=)	rs145660527	0.00006
NM_000996.4(RPL35A):c.11+17T>C	rs780298603	0.00001
NM_000996.4(RPL35A):c.282T>C (p.Ala94=)	rs201018840

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