List of variants in gene combination IGF1R, IRAIN reported as likely 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000875.5(IGF1R):c.16G>A (p.Gly6Arg)	rs199652097	0.00015
NM_000875.5(IGF1R):c.84G>A (p.Thr28=)	rs372748482	0.00013
NM_000875.5(IGF1R):c.94+15G>A	rs139440044	0.00006
NM_000875.5(IGF1R):c.75C>T (p.Leu25=)	rs749920743	0.00002
NM_000875.5(IGF1R):c.94+7A>G	rs201544675	0.00001
NM_000875.5(IGF1R):c.48C>A (p.Leu16=)	rs1319522971
NM_000875.5(IGF1R):c.60C>T (p.Ser20=)	rs2505322166
NM_000875.5(IGF1R):c.84G>C (p.Thr28=)
NM_000875.5(IGF1R):c.94+10_94+11del	rs746177297
NM_000875.5(IGF1R):c.94+17_94+23del

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