List of variants in gene WHRN 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: 12

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HGVS	dbSNP	gnomAD frequency
NM_015404.4(WHRN):c.1166+18G>A	rs149202009	0.00456
NM_015404.4(WHRN):c.2510G>A (p.Arg837His)	rs55749855	0.00053
NM_015404.4(WHRN):c.1148C>A (p.Thr383Asn)	rs147283064	0.00052
NM_015404.4(WHRN):c.1999G>A (p.Ala667Thr)	rs202161016	0.00010
NM_015404.4(WHRN):c.2571G>T (p.Gln857His)	rs776712642	0.00010
NM_015404.4(WHRN):c.35C>T (p.Ser12Leu)	rs760261757	0.00003
NM_015404.4(WHRN):c.1097G>A (p.Arg366His)	rs763238664	0.00001
NM_015404.4(WHRN):c.2453G>A (p.Arg818His)	rs762248099	0.00001
NM_015404.4(WHRN):c.2173G>A (p.Glu725Lys)	rs376805417
NM_015404.4(WHRN):c.2618G>A (p.Arg873Gln)	rs1301232723
NM_015404.4(WHRN):c.2722T>C (p.Ter908Gln)	rs727505255
NM_015404.4(WHRN):c.856dup (p.Asp286fs)	rs1064794551

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