List of variants in gene combination INS, INS-IGF2 reported as pathogenic for monogenic diabetes

Minimum submission review status:		Collection method:
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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: 13

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HGVS	dbSNP	gnomAD frequency
NM_000207.3(INS):c.16C>T (p.Arg6Cys)	rs121908278	0.00003
NM_000207.3(INS):c.125T>C (p.Val42Ala)	rs886037863
NM_000207.3(INS):c.127T>G (p.Cys43Gly)	rs80356666
NM_000207.3(INS):c.137G>A (p.Arg46Gln)	rs121908260
NM_000207.3(INS):c.143T>G (p.Phe48Cys)	rs80356668
NM_000207.3(INS):c.163C>T (p.Arg55Cys)	rs121908261
NM_000207.3(INS):c.187+241G>A	rs886041083
NM_000207.3(INS):c.188-31G>A	rs797045623
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.71C>A (p.Ala24Asp)	rs80356663
NM_000207.3(INS):c.94G>A (p.Gly32Ser)	rs80356664
NM_001042376.3(INS-IGF2):c.155C>T (p.Pro52Leu)	rs145038693

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