List of variants in gene FAM20C 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_020223.4(FAM20C):c.1228T>A (p.Ser410Thr)	rs148276213	0.00591
NM_020223.4(FAM20C):c.1505+20C>T	rs145973343	0.00455
NM_020223.4(FAM20C):c.1740C>T (p.Ala580=)	rs563226142	0.00273
NM_020223.4(FAM20C):c.1681G>A (p.Val561Met)	rs145750007	0.00213
NM_020223.4(FAM20C):c.731C>T (p.Pro244Leu)	rs116181849	0.00107
NM_020223.4(FAM20C):c.1748C>T (p.Ala583Val)	rs557222235	0.00024
NM_020223.4(FAM20C):c.458G>A (p.Gly153Asp)	rs751592577	0.00010
NM_020223.4(FAM20C):c.1690A>C (p.Asn564His)	rs36139924
NM_020223.4(FAM20C):c.784+19A>T	rs192542992

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