List of variants in gene INSR reported as uncertain significance for carbohydrate metabolism disease

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_000208.4(INSR):c.909G>A (p.Gln303=)	rs9282757	0.00950
NM_000208.4(INSR):c.1550A>G (p.Glu517Gly)	rs147671523	0.00058
NM_000208.4(INSR):c.2573C>T (p.Thr858Met)	rs201466857	0.00048
NM_000208.4(INSR):c.2388G>C (p.Arg796Ser)	rs78433961	0.00036
NM_000208.4(INSR):c.39G>C (p.Pro13=)	rs771984795	0.00029
NM_000208.4(INSR):c.2665C>T (p.Arg889Trp)	rs76077021	0.00021
NM_000208.4(INSR):c.3193C>G (p.Leu1065Val)	rs56395521	0.00021
NM_000208.4(INSR):c.3775G>A (p.Asp1259Asn)	rs369102740	0.00007
NM_000208.4(INSR):c.1628C>T (p.Thr543Met)	rs767160876	0.00006
NM_000208.4(INSR):c.3143G>A (p.Gly1048Asp)	rs200921389	0.00005
NM_000208.4(INSR):c.2121C>T (p.Gly707=)	rs753257847	0.00002
NM_000208.4(INSR):c.14G>A (p.Gly5Asp)	rs886054690	0.00001
NM_000208.4(INSR):c.2498G>A (p.Arg833Gln)	rs777565396	0.00001
NM_000208.4(INSR):c.1973T>G (p.Phe658Cys)
NM_000208.4(INSR):c.3410T>C (p.Ile1137Thr)	rs775854644
NM_000208.4(INSR):c.704G>T (p.Cys235Phe)

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