List of variants in gene MLXIPL reported as benign by Labcorp Genetics (formerly Invitae), Labcorp

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: 23

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HGVS	dbSNP	gnomAD frequency
NM_032951.3(MLXIPL):c.1095C>A (p.Pro365=)	rs112990540	0.03202
NM_032951.3(MLXIPL):c.732C>A (p.Asp244Glu)	rs34922362	0.01886
NM_032951.3(MLXIPL):c.2124G>A (p.Ala708=)	rs74447564	0.01346
NM_032951.3(MLXIPL):c.1096T>C (p.Leu366=)	rs190197045	0.00595
NM_032951.3(MLXIPL):c.444C>G (p.Pro148=)	rs72649027	0.00529
NM_032951.3(MLXIPL):c.573+7G>A	rs200438567	0.00354
NM_032951.3(MLXIPL):c.1563G>A (p.Ala521=)	rs200967567	0.00323
NM_032951.3(MLXIPL):c.620C>T (p.Ala207Val)	rs61746652	0.00304
NM_032951.3(MLXIPL):c.1198C>G (p.Pro400Ala)	rs186788005	0.00291
NM_032951.3(MLXIPL):c.874A>C (p.Ser292Arg)	rs6948907	0.00290
NM_032951.3(MLXIPL):c.483+8G>A	rs72649026	0.00285
NM_032951.3(MLXIPL):c.594A>G (p.Glu198=)	rs138119872	0.00278
NM_032951.3(MLXIPL):c.1537G>A (p.Ala513Thr)	rs200391124	0.00214
NM_032951.3(MLXIPL):c.2272G>A (p.Val758Ile)	rs72649012	0.00119
NM_032951.3(MLXIPL):c.1554C>G (p.Pro518=)	rs200441433	0.00035
NM_032951.3(MLXIPL):c.22C>T (p.Leu8=)	rs557125342	0.00028
NM_032951.3(MLXIPL):c.573+8G>C	rs569304409	0.00023
NM_032951.3(MLXIPL):c.1483C>T (p.Pro495Ser)	rs368147395	0.00017
NM_032951.3(MLXIPL):c.1467C>A (p.Ser489=)	rs563363573	0.00014
NM_032951.3(MLXIPL):c.2490C>T (p.Thr830=)	rs149935648	0.00014
NM_032951.3(MLXIPL):c.293+6G>A	rs552633036	0.00014
NM_032951.3(MLXIPL):c.1671+10C>T	rs372647137	0.00011
NM_032951.3(MLXIPL):c.1715C>A (p.Thr572Asn)	rs199616981

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