ClinVar Miner

List of variants in gene INS reported 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
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000207.2(INS):c.-139A>G	rs571342427	0.00080
NM_000207.2(INS):c.-147del	rs563630291
NM_000207.2(INS):c.-187_-164del	rs1135401727
NM_000207.3(INS):c.-152C>G	rs748749585

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