List of variants in gene combination CHM, LOC129391306 reported as uncertain significance by Ambry 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_000390.4(CHM):c.365A>G (p.His122Arg)	rs765999807	0.00003
NM_000390.4(CHM):c.352C>G (p.Leu118Val)	rs1355442853	0.00002
NM_000390.4(CHM):c.368C>T (p.Ala123Val)	rs372532715	0.00002
NM_000390.4(CHM):c.337G>A (p.Glu113Lys)	rs754548037	0.00001
NM_000390.4(CHM):c.397G>A (p.Ala133Thr)
NM_000390.4(CHM):c.481A>G (p.Ser161Gly)	rs748810856

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