List of variants in gene combination INS, INS-IGF2 reported by OMIM

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: 17

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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.266G>A (p.Arg89His)	rs28933985	0.00002
NM_000207.3(INS):c.100C>G (p.His34Asp)	rs121918101
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>C (p.Phe48Ser)	rs80356668
NM_000207.3(INS):c.143T>G (p.Phe48Cys)	rs80356668
NM_000207.3(INS):c.147C>G (p.Phe49Leu)	rs148685531
NM_000207.3(INS):c.163C>T (p.Arg55Cys)	rs121908261
NM_000207.3(INS):c.187+241G>A	rs886041083
NM_000207.3(INS):c.265C>T (p.Arg89Cys)	rs80356669
NM_000207.3(INS):c.266G>C (p.Arg89Pro)	rs28933985
NM_000207.3(INS):c.266G>T (p.Arg89Leu)	rs28933985
NM_000207.3(INS):c.274G>T (p.Val92Leu)	rs121918102
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

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