List of variants in gene GRN 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: 26

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HGVS	dbSNP	gnomAD frequency
NM_002087.4(GRN):c.384T>C (p.Asp128=)	rs25646	0.02616
NM_002087.4(GRN):c.1544G>C (p.Gly515Ala)	rs25647	0.00781
NM_002087.4(GRN):c.545C>T (p.Thr182Met)	rs63750479	0.00356
NM_002087.4(GRN):c.1227G>A (p.Thr409=)	rs140298583	0.00326
NM_002087.4(GRN):c.1298G>A (p.Arg433Gln)	rs114248177	0.00247
NM_002087.4(GRN):c.1253G>A (p.Arg418Gln)	rs63751100	0.00022
NM_002087.4(GRN):c.1555G>A (p.Val519Met)	rs141111290	0.00010
NM_002087.4(GRN):c.415T>C (p.Cys139Arg)	rs763841075	0.00010
NM_002087.4(GRN):c.497C>T (p.Pro166Leu)	rs368705304	0.00009
NM_002087.4(GRN):c.53C>T (p.Thr18Met)	rs199572314	0.00009
NM_002087.4(GRN):c.229G>A (p.Val77Ile)	rs148531161	0.00008
NM_002087.4(GRN):c.626C>T (p.Pro209Leu)	rs368995988	0.00008
NM_002087.4(GRN):c.1540G>A (p.Val514Met)	rs142926942	0.00005
NM_002087.4(GRN):c.1648G>A (p.Val550Ile)	rs63750754	0.00004
NM_002087.4(GRN):c.1485C>T (p.Cys495=)	rs63750576	0.00003
NM_002087.4(GRN):c.302G>A (p.Arg101Gln)	rs201686997	0.00003
NM_002087.4(GRN):c.1373C>T (p.Pro458Leu)	rs63750537	0.00002
NM_002087.4(GRN):c.208G>A (p.Gly70Ser)	rs772381732	0.00002
NM_002087.4(GRN):c.530G>A (p.Arg177His)	rs753441122	0.00002
NM_002087.4(GRN):c.1288C>G (p.Pro430Ala)	rs200645022	0.00001
NM_002087.4(GRN):c.1352C>T (p.Pro451Leu)	rs752428000	0.00001
NM_002087.4(GRN):c.22G>A (p.Val8Met)	rs774367010	0.00001
NM_002087.4(GRN):c.58T>C (p.Cys20Arg)	rs542613543	0.00001
NM_002087.4(GRN):c.1036_1038del (p.Glu346del)	rs751373342
NM_002087.4(GRN):c.301C>T (p.Arg101Trp)	rs543578531
NM_002087.4(GRN):c.352AAC[1] (p.Asn119del)	rs758168578

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