List of variants in gene ACTG2 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: 14

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HGVS	dbSNP	gnomAD frequency
NM_001615.4(ACTG2):c.126+5G>A	rs761722608	0.00001
NM_001615.4(ACTG2):c.217G>C (p.Glu73Gln)	rs780136497	0.00001
NM_001615.4(ACTG2):c.629T>C (p.Val210Ala)	rs2104822473	0.00001
NM_001615.4(ACTG2):c.805+4A>G	rs1188664556	0.00001
NM_001615.4(ACTG2):c.1034C>G (p.Ser345Cys)	rs1553397067
NM_001615.4(ACTG2):c.1037T>C (p.Ile346Thr)	rs2104827803
NM_001615.4(ACTG2):c.1068G>T (p.Met356Ile)	rs2466922204
NM_001615.4(ACTG2):c.137T>C (p.Val46Ala)	rs2466893610
NM_001615.4(ACTG2):c.455T>A (p.Ile152Asn)
NM_001615.4(ACTG2):c.565T>C (p.Tyr189His)	rs1057520776
NM_001615.4(ACTG2):c.614C>T (p.Ala205Val)	rs1680222160
NM_001615.4(ACTG2):c.637A>G (p.Ile213Val)	rs1680222670
NM_001615.4(ACTG2):c.793C>T (p.Pro265Ser)
NM_001615.4(ACTG2):c.811G>A (p.Glu271Lys)	rs2104825018

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