List of variants in gene combination INS, INS-IGF2 reported as benign by Clinical Genomics, Uppaluri K&H Personalized Medicine Clinic

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: 14

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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.188-96G>A	rs565314634	0.00016
NM_000207.3(INS):c.*2C>T	rs200306755	0.00013
NM_000207.3(INS):c.*28G>A	rs778107057	0.00006
NM_000207.3(INS):c.*42C>T	rs376867722	0.00006
NM_000207.3(INS):c.-18+22G>A	rs1051986248	0.00001
NM_000207.3(INS):c.-17-70G>A	rs1554920985
NM_000207.3(INS):c.-18+21C>T	rs568856178
NM_000207.3(INS):c.-18+3C>G	rs886048112
NM_000207.3(INS):c.153A>C (p.Thr51=)	rs773789432
NM_000207.3(INS):c.187+15C>T	rs754089310
NM_000207.3(INS):c.72C>A (p.Ala24=)	rs539284976

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