"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "LIFR"[g - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1943062	NM_001127671.2(LIFR):c.3290A>T (p.Asp1097Val)	LIFR (D1097V +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2202098	NM_001127671.2(LIFR):c.3289G>A (p.Asp1097Asn)	LIFR (D1097N +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 353605	NM_001127671.2(LIFR):c.3288C>A (p.Asn1096Lys)	LIFR (N1096K +1 more)	Single nucleotide variant (missense variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 195484	NM_001127671.2(LIFR):c.3288C>T (p.Asn1096=)	LIFR	Single nucleotide variant (synonymous variant)	Stüve-Wiedemann syndrome 1 +3 more	GBenign/Likely benign
Select item 1991071	NM_001127671.2(LIFR):c.3285A>G (p.Pro1095=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 353606	NM_001127671.2(LIFR):c.3279C>T (p.Asn1093=)	LIFR	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1053132	NM_001127671.2(LIFR):c.3275A>G (p.Gln1092Arg)	LIFR (Q1081R +1 more)	Single nucleotide variant (missense variant)	Stüve-Wiedemann syndrome 1 +1 more	GUncertain significance
Select item 1936396	NM_001127671.2(LIFR):c.3267C>G (p.Asn1089Lys)	LIFR (N1078K +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1111073	NM_001127671.2(LIFR):c.3264A>G (p.Thr1088=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1948121	NM_001127671.2(LIFR):c.3254G>A (p.Trp1085Ter)	LIFR (W1074* +1 more)	Single nucleotide variant (nonsense)	Stüve-Wiedemann syndrome 1 +1 more	GUncertain significance
Select item 1620501	NM_001127671.2(LIFR):c.3252G>A (p.Gly1084=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2803886	NM_001127671.2(LIFR):c.3246A>C (p.Gly1082=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2706385	NM_001127671.2(LIFR):c.3246A>T (p.Gly1082=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1416697	NM_001127671.2(LIFR):c.3245G>A (p.Gly1082Glu)	LIFR (G1071E +1 more)	Single nucleotide variant (missense variant)	Stüve-Wiedemann syndrome 1 +1 more	GUncertain significance
Select item 2034985	NM_001127671.2(LIFR):c.3243T>C (p.Asn1081=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2018262	NM_001127671.2(LIFR):c.3240T>C (p.Ser1080=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2886764	NM_001127671.2(LIFR):c.3234T>C (p.Pro1078=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1356601	NM_001127671.2(LIFR):c.3231_3232del (p.Ser1077_Pro1078insTer)	LIFR	Microsatellite (frameshift variant)	not provided +1 more	GUncertain significance
Select item 2824897	NM_001127671.2(LIFR):c.3231T>A (p.Ser1077=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2820268	NM_001127671.2(LIFR):c.3222T>C (p.Asp1074=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 618197	NM_001127671.2(LIFR):c.3221A>G (p.Asp1074Gly)	LIFR (D1074G +1 more)	Single nucleotide variant (missense variant)	Stuve-Wiedemann syndrome +3 more	GConflicting classifications of pathogenicity
Select item 2138948	NM_001127671.2(LIFR):c.3217A>G (p.Lys1073Glu)	LIFR (K1073E +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2911470	NM_001127671.2(LIFR):c.3213T>C (p.Pro1071=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2984224	NM_001127671.2(LIFR):c.3210T>A (p.Ile1070=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1514746	NM_001127671.2(LIFR):c.3197G>A (p.Arg1066Gln)	LIFR (R1055Q +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2103984	NM_001127671.2(LIFR):c.3183C>T (p.Cys1061=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1653906	NM_001127671.2(LIFR):c.3180A>G (p.Pro1060=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2710368	NM_001127671.2(LIFR):c.3174A>C (p.Gly1058=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2030581	NM_001127671.2(LIFR):c.3174A>G (p.Gly1058=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2869269	NM_001127671.2(LIFR):c.3168A>C (p.Ser1056=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2150048	NM_001127671.2(LIFR):c.3166T>C (p.Ser1056Pro)	LIFR (S1056P +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2884223	NM_001127671.2(LIFR):c.3162T>C (p.Ile1054=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2103050	NM_001127671.2(LIFR):c.3156T>C (p.Ser1052=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1091280	NM_001127671.2(LIFR):c.3147C>T (p.Asp1049=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 797713	NM_001127671.2(LIFR):c.3132T>C (p.Ser1044=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1362710	NM_001127671.2(LIFR):c.3131C>T (p.Ser1044Phe)	LIFR (S1033F +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1627797	NM_001127671.2(LIFR):c.3114T>C (p.Asn1038=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2772605	NM_001127671.2(LIFR):c.3108A>T (p.Thr1036=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1669709	NM_001127671.2(LIFR):c.3108A>G (p.Thr1036=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1667013	NM_001127671.2(LIFR):c.3105T>C (p.Asn1035=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2984548	NM_001127671.2(LIFR):c.3102A>G (p.Val1034=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2782005	NM_001127671.2(LIFR):c.3099T>C (p.Asn1033=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 981877	NM_001127671.2(LIFR):c.3089C>T (p.Pro1030Leu)	LIFR (P1019L +1 more)	Single nucleotide variant (missense variant)	Hereditary breast ovarian cancer syndrome +1 more	GUncertain significance
Select item 618703	NM_001127671.2(LIFR):c.3087A>G (p.Arg1029=)	LIFR	Single nucleotide variant (synonymous variant)	Stuve-Wiedemann syndrome +1 more	GLikely benign
Select item 1702460	NM_001127671.2(LIFR):c.3086G>A (p.Arg1029Lys)	LIFR (R1018K +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 797005	NM_001127671.2(LIFR):c.3084C>T (p.Tyr1028=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1129548	NM_001127671.2(LIFR):c.3078G>C (p.Ala1026=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 763349	NM_001127671.2(LIFR):c.3078G>A (p.Ala1026=)	LIFR	Single nucleotide variant (synonymous variant)	Connective tissue disorder +1 more	GConflicting classifications of pathogenicity
Select item 2149151	NM_001127671.2(LIFR):c.3077C>T (p.Ala1026Val)	LIFR (A1015V +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 763325	NM_001127671.2(LIFR):c.3060G>A (p.Glu1020=)	LIFR	Single nucleotide variant (synonymous variant)	Stuve-Wiedemann syndrome +1 more	GConflicting classifications of pathogenicity
Select item 2742851	NM_001127671.2(LIFR):c.3048A>C (p.Ile1016=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 791443	NM_001127671.2(LIFR):c.3039G>C (p.Val1013=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1921010	NM_001127671.2(LIFR):c.3033T>C (p.Ser1011=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1385099	NM_001127671.2(LIFR):c.3015G>A (p.Met1005Ile)	LIFR (M1005I +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1134242	NM_001127671.2(LIFR):c.3009A>C (p.Pro1003=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2164181	NM_001127671.2(LIFR):c.3002A>G (p.Tyr1001Cys)	LIFR (Y990C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2822223	NM_001127671.2(LIFR):c.3000C>T (p.Gly1000=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1630522	NM_001127671.2(LIFR):c.3000C>A (p.Gly1000=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2193868	NM_001127671.2(LIFR):c.2995G>T (p.Ala999Ser)	LIFR (A988S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1994386	NM_001127671.2(LIFR):c.2991A>G (p.Gly997=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1602493	NM_001127671.2(LIFR):c.2985T>C (p.Pro995=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1046143	NM_001127671.2(LIFR):c.2962GAA[2] (p.Glu990del)	LIFR (E979del +1 more)	Microsatellite (inframe_deletion)	not provided	GUncertain significance
Select item 2176473	NM_001127671.2(LIFR):c.2968G>C (p.Glu990Gln)	LIFR (E979Q +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2820695	NM_001127671.2(LIFR):c.2955A>C (p.Ala985=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2169944	NM_001127671.2(LIFR):c.2952A>G (p.Gln984=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1956215	NM_001127671.2(LIFR):c.2949T>G (p.Pro983=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1191489	NM_001127671.2(LIFR):c.2948C>G (p.Pro983Arg)	LIFR (P972R +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 593625	NM_001127671.2(LIFR):c.2937G>A (p.Ser979=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GConflicting classifications of pathogenicity
Select item 353608	NM_001127671.2(LIFR):c.2934G>A (p.Gln978=)	LIFR	Single nucleotide variant (synonymous variant)	not specified +4 more	GConflicting classifications of pathogenicity
Select item 2076414	NM_001127671.2(LIFR):c.2922C>T (p.Tyr974=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1080641	NM_001127671.2(LIFR):c.2910A>G (p.Ala970=)	LIFR	Single nucleotide variant (synonymous variant)	Stüve-Wiedemann syndrome 1 +1 more	GLikely benign
Select item 1080330	NM_001127671.2(LIFR):c.2910A>C (p.Ala970=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1606262	NM_001127671.2(LIFR):c.2904G>C (p.Gly968=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1122675	NM_001127671.2(LIFR):c.2895A>G (p.Glu965=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1055784	NM_001127671.2(LIFR):c.2887G>A (p.Ala963Thr)	LIFR (A952T +1 more)	Single nucleotide variant (missense variant)	Stüve-Wiedemann syndrome 1 +1 more	GUncertain significance
Select item 740990	NM_001127671.2(LIFR):c.2886C>T (p.Ala962=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2199791	NM_001127671.2(LIFR):c.2875C>A (p.Pro959Thr)	LIFR (P959T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1128545	NM_001127671.2(LIFR):c.2844C>G (p.Ser948=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2758451	NM_001127671.2(LIFR):c.2835G>C (p.Val945=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1151761	NM_001127671.2(LIFR):c.2832T>C (p.His944=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1123719	NM_001127671.2(LIFR):c.2808C>T (p.Arg936=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 795337	NM_001127671.2(LIFR):c.2799T>C (p.Pro933=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2151158	NM_001127671.2(LIFR):c.2794C>T (p.Arg932Cys)	LIFR (R921C +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2037968	NM_001127671.2(LIFR):c.2781C>T (p.Ser927=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1159187	NM_001127671.2(LIFR):c.2781C>A (p.Ser927=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2757151	NM_001127671.2(LIFR):c.2778T>A (p.Ile926=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 353610	NM_001127671.2(LIFR):c.2766T>C (p.Asp922=)	LIFR	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 2188584	NM_001127671.2(LIFR):c.2759T>C (p.Ile920Thr)	LIFR (I909T +1 more)	Single nucleotide variant (missense variant)	Stüve-Wiedemann syndrome 1 +1 more	GUncertain significance
Select item 1985161	NM_001127671.2(LIFR):c.2744C>T (p.Ser915Leu)	LIFR (S904L +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2200663	NM_001127671.2(LIFR):c.2741G>A (p.Arg914Gln)	LIFR (R914Q +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2033410	NM_001127671.2(LIFR):c.2733G>A (p.Leu911=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2147544	NM_001127671.2(LIFR):c.2720A>G (p.Asn907Ser)	LIFR (N907S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +2 more	GUncertain significance
Select item 1636313	NM_001127671.2(LIFR):c.2715A>G (p.Pro905=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1966489	NM_001127671.2(LIFR):c.2712C>T (p.Thr904=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2974418	NM_001127671.2(LIFR):c.2706T>C (p.Pro902=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2021713	NM_001127671.2(LIFR):c.2694G>A (p.Leu898=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 904838	NM_001127671.2(LIFR):c.2692T>C (p.Leu898=)	LIFR	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1573726	NM_001127671.2(LIFR):c.2688A>G (p.Lys896=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1414247	NM_001127671.2(LIFR):c.2683C>T (p.Leu895Phe)	LIFR (L884F +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1541038	NM_001127671.2(LIFR):c.2682T>C (p.Ala894=)	LIFR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

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