List of variants in gene EMC1 reported as likely benign by Fulgent Genetics, Fulgent 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_015047.3(EMC1):c.2886C>T (p.Tyr962=)	rs34350799	0.00555
NM_015047.3(EMC1):c.787-13T>C	rs143475773	0.00342
NM_015047.3(EMC1):c.884T>C (p.Leu295Ser)	rs3850531	0.00287
NM_015047.3(EMC1):c.2065-4C>T	rs777919151	0.00001

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