List of variants in gene DRC1 reported as uncertain significance 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_145038.5(DRC1):c.1418C>T (p.Ala473Val)	rs199574440	0.00029
NM_145038.5(DRC1):c.421T>G (p.Trp141Gly)	rs139583194	0.00023
NM_145038.5(DRC1):c.1913A>C (p.Lys638Thr)	rs142671417	0.00014
NM_145038.5(DRC1):c.1391G>A (p.Arg464His)	rs200271366	0.00004
NM_145038.5(DRC1):c.2079_2086del (p.Arg694fs)	rs1558457993
NM_145038.5(DRC1):c.2190_2193dup (p.Thr732fs)	rs763631774

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