List of variants in gene FIG4 reported as uncertain significance by Centre for Mendelian Genomics, University Medical Centre Ljubljana

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_014845.6(FIG4):c.122T>C (p.Ile41Thr)	rs121908287	0.00117
NM_014845.6(FIG4):c.1751-16A>G	rs200778905	0.00026
NM_014845.6(FIG4):c.2096G>A (p.Arg699His)	rs750091928	0.00007
NM_014845.6(FIG4):c.2095C>T (p.Arg699Cys)	rs764799053	0.00004
NM_014845.6(FIG4):c.2018T>A (p.Ile673Asn)	rs774499394	0.00001

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