List of variants in gene LINS1 reported as uncertain significance by Genetic Services Laboratory, University of Chicago

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_001040616.3(LINS1):c.864C>T (p.Thr288=)	rs150775570	0.00051
NM_001040616.3(LINS1):c.1347G>A (p.Met449Ile)	rs201677311	0.00005
NM_001040616.3(LINS1):c.569G>T (p.Cys190Phe)	rs779712690	0.00003
NM_001040616.3(LINS1):c.848T>A (p.Met283Lys)	rs780141210	0.00002
NM_001040616.3(LINS1):c.1394+4A>G	rs200846434
NM_001040616.3(LINS1):c.1632C>T (p.Asn544=)	rs772619184
NM_001040616.3(LINS1):c.1912G>A (p.Glu638Lys)	rs797045682
NM_001040616.3(LINS1):c.2236A>G (p.Ile746Val)	rs587780380

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