List of variants in gene combination INS, INS-IGF2 reported 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
		ClinVar version:

Total variants: 32

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HGVS	dbSNP	gnomAD frequency
NM_000207.3(INS):c.188-16C>T	rs5507	0.00616
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.147C>T (p.Phe49=)	rs148685531	0.00016
NM_000207.3(INS):c.188-96G>A	rs565314634	0.00016
NM_000207.3(INS):c.188-233C>T	rs970395863	0.00007
NM_000207.3(INS):c.-46A>G	rs772426967	0.00004
NM_000207.3(INS):c.-18+22G>A	rs1051986248	0.00001
NM_000207.3(INS):c.188-137A>T	rs1378546387	0.00001
NM_000207.3(INS):c.-17-70G>A	rs1554920985
NM_000207.3(INS):c.-17-74T>C	rs9282755
NM_000207.3(INS):c.-18+21C>T	rs568856178
NM_000207.3(INS):c.-18+62C>T	rs1166335966
NM_000207.3(INS):c.103C>G (p.Leu35Val)	rs1278232284
NM_000207.3(INS):c.153A>G (p.Thr51=)	rs773789432
NM_000207.3(INS):c.163C>T (p.Arg55Cys)	rs121908261
NM_000207.3(INS):c.187+271A>G	rs1845862881
NM_000207.3(INS):c.187+391C>T
NM_000207.3(INS):c.188-31G>A	rs797045623
NM_000207.3(INS):c.188-97C>T	rs746839746
NM_000207.3(INS):c.265C>T (p.Arg89Cys)	rs80356669
NM_000207.3(INS):c.289A>C (p.Thr97Pro)	rs2133672927
NM_000207.3(INS):c.292A>T (p.Ser98Cys)	rs1252051752
NM_000207.3(INS):c.299G>A (p.Cys100Tyr)
NM_000207.3(INS):c.308A>G (p.Tyr103Cys)	rs121908277
NM_000207.3(INS):c.320ACT[1] (p.Tyr108del)	rs1554920552
NM_000207.3(INS):c.71C>A (p.Ala24Asp)	rs80356663
NM_000207.3(INS):c.71C>T (p.Ala24Val)	rs80356663
NM_000207.3(INS):c.94G>A (p.Gly32Ser)	rs80356664
NM_000207.3(INS):c.95G>T (p.Gly32Val)	rs2133676747

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