List of variants in gene RHBDF2 reported as likely benign by Illumina Laboratory Services, Illumina

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_024599.5(RHBDF2):c.-297C>T	rs571688447	0.00146
NM_001005498.4(RHBDF2):c.31G>A (p.Val11Met)	rs142019309	0.00018
NM_001005498.4(RHBDF2):c.680C>T (p.Ser227Leu)	rs143672318	0.00011
NM_001005498.4(RHBDF2):c.359T>C (p.Met120Thr)	rs367658130	0.00005
NM_001005498.4(RHBDF2):c.327G>T (p.Gln109His)	rs763124357	0.00004
NM_001005498.4(RHBDF2):c.391C>T (p.Arg131Cys)	rs751482282	0.00003
NM_001005498.4(RHBDF2):c.1235G>A (p.Arg412Gln)	rs377416669	0.00002
NM_001005498.4(RHBDF2):c.1574+7C>T	rs568757638	0.00001
NM_001005498.4(RHBDF2):c.617G>C (p.Arg206Pro)	rs145040227

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