List of variants in gene INS studied for not specified

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: 7

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HGVS	dbSNP	gnomAD frequency
NC_000011.10:g.2161289T>C	rs571342427	0.00074
NM_000207.2(INS):c.-293C>T	rs562867858	0.00020
NM_000207.3(INS):c.-153C>G	rs915076855	0.00019
NM_000207.2(INS):c.-146A>C	rs2133678050
NM_000207.2(INS):c.-379_-372dup	rs1329632206
NM_000207.2(INS):c.-88A>G	rs2133677909
NM_000207.3(INS):c.-152C>G	rs748749585

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