List of variants in gene combination INS, INS-IGF2, TH reported as uncertain significance for pancreas disorder

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_000207.3(INS):c.*22A>C	rs3842753	0.59307
NM_000207.3(INS):c.-18+4_-18+5insTTGC	rs3842740	0.07357

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