List of variants in gene INSR reported by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_000208.4(INSR):c.2293G>A (p.Gly765Ser)	rs146698985	0.00036
NM_000208.4(INSR):c.224A>G (p.Asp75Gly)	rs142910337	0.00025
NM_000208.4(INSR):c.3143G>A (p.Gly1048Asp)	rs200921389	0.00007
NM_000208.4(INSR):c.2599G>A (p.Val867Ile)	rs766938463	0.00002
NM_000208.4(INSR):c.1151A>G (p.Asn384Ser)	rs1419106670	0.00001
NM_000208.4(INSR):c.3312G>A (p.Glu1104=)	rs1445698616	0.00001
NC_000019.9:g.(?_7112275)_(7123001_7125293)dup
NM_000208.4(INSR):c.1477G>T (p.Ala493Ser)
NM_000208.4(INSR):c.2364G>T (p.Val788=)
NM_000208.4(INSR):c.3058C>T (p.Arg1020Ter)
NM_000208.4(INSR):c.3868C>T (p.Leu1290Phe)

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