List of variants in gene combination ARG1, MED23 reported as uncertain significance by GeneDx

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_000045.4(ARG1):c.798A>C (p.Lys266Asn)	rs111253965	0.00041
NM_000045.4(ARG1):c.472G>A (p.Asp158Asn)	rs751647696	0.00017
NM_000045.4(ARG1):c.237G>C (p.Gln79His)	rs148619575	0.00016
NM_000045.4(ARG1):c.944T>C (p.Ile315Thr)	rs202219126	0.00006
NM_000045.4(ARG1):c.482G>C (p.Gly161Ala)	rs201484132	0.00005
NM_000045.4(ARG1):c.892G>C (p.Ala298Pro)	rs755359126	0.00004
NM_000045.4(ARG1):c.266A>C (p.Lys89Thr)	rs759832639	0.00001
NM_000045.4(ARG1):c.827T>C (p.Met276Thr)	rs1395352972	0.00001
NM_000045.4(ARG1):c.926A>G (p.Glu309Gly)	rs775225648	0.00001
NM_000045.4(ARG1):c.196A>G (p.Ile66Val)
NM_000045.4(ARG1):c.75A>C (p.Glu25Asp)	rs755973004
NM_000045.4(ARG1):c.770G>T (p.Gly257Val)	rs772473981

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