List of variants in gene VIM reported as likely benign for cataract

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_003380.5(VIM):c.542A>C (p.Asp181Ala)	rs149942621	0.00115
NM_003380.5(VIM):c.749A>G (p.Gln250Arg)	rs145152785	0.00111
NM_003380.5(VIM):c.987A>G (p.Glu329=)	rs147429387	0.00026
NM_003380.5(VIM):c.384T>C (p.Asn128=)	rs147857896	0.00016
NM_003380.5(VIM):c.1360-17T>G	rs764183925	0.00010
NM_003380.5(VIM):c.1009-8C>A	rs372984113	0.00003
NM_003380.5(VIM):c.1122G>A (p.Glu374=)
NM_003380.5(VIM):c.1360-18G>T
NM_003380.5(VIM):c.1368C>T (p.Asn456=)
NM_003380.5(VIM):c.423A>G (p.Gln141=)	rs2131679660
NM_003380.5(VIM):c.624+17C>G
NM_003380.5(VIM):c.624+7A>C	rs376197279
NM_003380.5(VIM):c.624+7A>G
NM_003380.5(VIM):c.882+20G>A
NM_003380.5(VIM):c.990G>C (p.Val330=)

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