List of variants in gene INSR, LOC129391047 studied for autosomal recessive disease

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000208.4(INSR):c.*3623A>G	rs77859571	0.04400
NM_000208.4(INSR):c.*3592A>G	rs75499056	0.01497
NM_000208.4(INSR):c.*3541C>T	rs116953519	0.00271
NM_000208.4(INSR):c.*3654G>A	rs753611294	0.00032
NM_000208.4(INSR):c.*3685T>C	rs143409422	0.00025

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