List of variants in gene FYCO1 reported as uncertain significance for not provided

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_024513.4(FYCO1):c.*1445C>T	rs143753654	0.00148
NM_024513.4(FYCO1):c.4394C>T (p.Thr1465Met)	rs201764993	0.00038
NM_024513.4(FYCO1):c.452T>C (p.Val151Ala)	rs142081868	0.00035
NM_024513.4(FYCO1):c.4321C>A (p.Pro1441Thr)	rs185127002	0.00033
NM_024513.4(FYCO1):c.2815G>C (p.Ala939Pro)	rs531750827	0.00019
NM_024513.4(FYCO1):c.443C>T (p.Ser148Leu)	rs149818406	0.00016
NM_024513.4(FYCO1):c.*176C>T	rs544729621	0.00009
NM_024513.4(FYCO1):c.4007C>T (p.Ser1336Leu)	rs4356851	0.00005
NM_024513.4(FYCO1):c.2695_2696insTT	rs145514188
NM_024513.4(FYCO1):c.1493A>C (p.Gln498Pro)	rs2528981180
NM_024513.4(FYCO1):c.364C>G (p.Gln122Glu)	rs779617235
NM_024513.4(FYCO1):c.3993C>T (p.Pro1331=)	rs752606656

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