List of variants in gene combination CHM, LOC129391306 reported as benign for not provided

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000390.4(CHM):c.351A>G (p.Ala117=)	rs10217950	0.16853
NM_000390.4(CHM):c.315-6T>C	rs377234801	0.00010
NM_000390.4(CHM):c.387C>T (p.Asn129=)	rs776758268	0.00002
NM_000390.4(CHM):c.483C>T (p.Ser161=)	rs779693887	0.00002
NM_000390.4(CHM):c.447G>T (p.Met149Ile)	rs746057999

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