ClinVar Miner

List of variants reported as likely benign for cataract 18 by Invitae

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 15
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HGVS dbSNP
NM_024513.4(FYCO1):c.108G>A (p.Thr36=) rs558777911
NM_024513.4(FYCO1):c.1248G>A (p.Lys416=) rs149643762
NM_024513.4(FYCO1):c.1659C>T (p.Leu553=) rs746026639
NM_024513.4(FYCO1):c.1985C>T (p.Ser662Phe) rs150785981
NM_024513.4(FYCO1):c.2006G>A (p.Ser669Asn) rs141155944
NM_024513.4(FYCO1):c.2199C>T (p.Leu733=)
NM_024513.4(FYCO1):c.2844G>A (p.Glu948=) rs182162227
NM_024513.4(FYCO1):c.2865G>A (p.Gln955=) rs1575368474
NM_024513.4(FYCO1):c.3215C>T (p.Ala1072Val)
NM_024513.4(FYCO1):c.3322A>G (p.Lys1108Glu) rs73830668
NM_024513.4(FYCO1):c.3438-9_3438-8del
NM_024513.4(FYCO1):c.3825G>A (p.Pro1275=) rs748985200
NM_024513.4(FYCO1):c.3903A>G (p.Thr1301=) rs144525738
NM_024513.4(FYCO1):c.4254C>A (p.Val1418=) rs1553620269
NM_024513.4(FYCO1):c.753G>T (p.Glu251Asp) rs3821885

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