List of variants in gene LIFR reported as uncertain significance by Eurofins NTD LLC (GA)

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_001127671.2(LIFR):c.364A>G (p.Thr122Ala)	rs145163157	0.00131
NM_001127671.2(LIFR):c.2302A>G (p.Arg768Gly)	rs139848756	0.00107
NM_001127671.2(LIFR):c.452C>G (p.Ser151Cys)	rs61751712	0.00015
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.1485T>C (p.Ala495=)	rs759537735	0.00002
NM_001127671.2(LIFR):c.1357T>C (p.Trp453Arg)	rs201516825	0.00001
NM_001127671.2(LIFR):c.1182ATT[2] (p.Leu396del)	rs754991843

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