List of variants in gene combination INS, INS-IGF2 reported as likely pathogenic by Molecular Genetics, Madras Diabetes Research Foundation

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_000207.3(INS):c.101A>C (p.His34Pro)	rs1564912274
NM_000207.3(INS):c.103C>A (p.Leu35Met)	rs1278232284
NM_000207.3(INS):c.143T>G (p.Phe48Cys)	rs80356668
NM_000207.3(INS):c.265C>T (p.Arg89Cys)	rs80356669
NM_000207.3(INS):c.287G>A (p.Cys96Tyr)	rs80356671
NM_000207.3(INS):c.293G>T (p.Ser98Ile)	rs2133672883
NM_000207.3(INS):c.322T>G (p.Tyr108Asp)	rs2133672778
NM_000207.3(INS):c.326G>T (p.Cys109Phe)	rs2133672742
NM_000207.3(INS):c.94G>A (p.Gly32Ser)	rs80356664

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