List of variants in gene combination INS, INS-IGF2 reported as likely benign by Genetic Services Laboratory, University of Chicago

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_000207.3(INS):c.188-10G>A	rs41275198	0.00262
NM_000207.3(INS):c.188-220C>T	rs561372758	0.00113
NM_000207.3(INS):c.188-114G>T	rs529554227	0.00029
NM_000207.3(INS):c.187+203G>A	rs147024795	0.00019
NM_000207.3(INS):c.-18+21C>T	rs568856178
NM_000207.3(INS):c.187+391C>T

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