List of variants in gene LMF1 reported as likely pathogenic for not provided

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_022773.4(LMF1):c.295C>T (p.Gln99Ter)	rs752473648	0.00009
NM_022773.4(LMF1):c.514G>A (p.Gly172Arg)	rs201406396	0.00005
NM_022773.4(LMF1):c.1323del (p.Phe441fs)	rs760536168	0.00004
NM_022773.4(LMF1):c.895C>T (p.Gln299Ter)	rs554054538	0.00004
NM_022773.4(LMF1):c.359C>G (p.Ser120Ter)	rs768161861	0.00001
NM_022773.4(LMF1):c.697C>T (p.Arg233Ter)	rs199953320	0.00001
NM_022773.4(LMF1):c.1022_1023insT (p.Arg342fs)	rs2151701732
NM_022773.4(LMF1):c.1374C>A (p.Tyr458Ter)	rs908611545
NM_022773.4(LMF1):c.1530-2A>G
NM_022773.4(LMF1):c.410C>T (p.Ser137Leu)
NM_022773.4(LMF1):c.465G>A (p.Trp155Ter)	rs975431860
NM_022773.4(LMF1):c.938G>A (p.Trp313Ter)

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