ClinVar Miner

List of variants in gene combination INS, INS-IGF2, TH reported as likely benign for Autosomal recessive DOPA responsive dystonia

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000207.3(INS):c.36G>A (p.Ala12=)	rs3842744	0.01335
NM_000207.3(INS):c.-9C>T	rs5505	0.00878

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