List of variants in gene GCKR reported 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
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_001486.4(GCKR):c.1618C>T (p.Arg540Ter)	rs146053779	0.00117
NM_001486.4(GCKR):c.1433G>A (p.Arg478His)	rs141361209	0.00024
NM_001486.4(GCKR):c.548C>T (p.Ser183Phe)	rs151082324	0.00020
NM_001486.4(GCKR):c.1550G>A (p.Trp517Ter)	rs371460190	0.00005
NM_001486.4(GCKR):c.17_22dup (p.Arg6_Phe7dup)	rs748731892
NM_001486.4(GCKR):c.740C>T (p.Pro247Leu)	rs148025735

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