List of variants in gene BRME1 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001345843.2(BRME1):c.576T>G (p.Asp192Glu)	rs142863596	0.00018
NM_001345843.2(BRME1):c.196G>A (p.Ala66Thr)	rs145816906	0.00014
NM_001345843.2(BRME1):c.1639G>A (p.Ala547Thr)	rs147705428	0.00001
NM_001345843.2(BRME1):c.503A>G (p.Asp168Gly)	rs775589300	0.00001

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