List of variants in gene LINS1 reported as uncertain significance by GeneDx

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001040616.3(LINS1):c.1940G>A (p.Ser647Asn)	rs150317593	0.00073
NM_001040616.3(LINS1):c.154dup (p.Thr52fs)	rs752815035	0.00006
NM_001040616.3(LINS1):c.281C>T (p.Thr94Ile)	rs750281247	0.00001
NM_001040616.3(LINS1):c.1351G>A (p.Glu451Lys)
NM_001040616.3(LINS1):c.1861C>T (p.Arg621Trp)
NM_001040616.3(LINS1):c.431del (p.Leu144fs)	rs764442764
NM_001040616.3(LINS1):c.79G>A (p.Asp27Asn)

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