ClinVar Miner

List of variants in gene combination HNF1B, LOC126862549 reported as uncertain risk allele by Clinical Genomics, Uppaluri K&H Personalized Medicine Clinic

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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_000458.4(HNF1B):c.592A>C (p.Ser198Arg)	rs1321074352	0.00001
NM_000458.4(HNF1B):c.778G>A (p.Glu260Lys)	rs1568665613

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