Variants in gene LIFR with conflicting interpretations "uncertain significance" and "likely benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 12

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HGVS	dbSNP	gnomAD frequency
NM_001127671.2(LIFR):c.364A>G (p.Thr122Ala)	rs145163157	0.00131
NM_001127671.2(LIFR):c.670A>G (p.Ile224Val)	rs151282774	0.00108
NM_001127671.2(LIFR):c.2302A>G (p.Arg768Gly)	rs139848756	0.00107
NM_001127671.2(LIFR):c.2934G>A (p.Gln978=)	rs148354076	0.00082
NM_001127671.2(LIFR):c.2280G>A (p.Leu760=)	rs370455274	0.00010
NM_001127671.2(LIFR):c.2937G>A (p.Ser979=)	rs201711670	0.00008
NM_001127671.2(LIFR):c.2670+6C>G	rs898718526	0.00003
NM_001127671.2(LIFR):c.1485T>C (p.Ala495=)	rs759537735	0.00002
NM_001127671.2(LIFR):c.3060G>A (p.Glu1020=)	rs537706381	0.00001
NM_001127671.2(LIFR):c.819T>C (p.Ser273=)	rs756161883	0.00001
NM_001127671.2(LIFR):c.1245G>A (p.Pro415=)	rs139809889
NM_001127671.2(LIFR):c.3288C>A (p.Asn1096Lys)	rs3729751

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