ClinVar Miner

List of variants in gene combination C12orf43, HNF1A reported as likely 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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000545.8(HNF1A):c.*5G>A	rs112986697	0.00237
NM_000545.8(HNF1A):c.*391G>C	rs868177605	0.00006

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