List of variants in gene HNF1A reported as benign by PreventionGenetics, part of Exact Sciences

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_000545.8(HNF1A):c.51C>G (p.Leu17=)	rs1169289	0.42543
NM_000545.8(HNF1A):c.79A>C (p.Ile27Leu)	rs1169288	0.35489
NM_000545.8(HNF1A):c.1501+7G>A	rs2464195	0.30441
NM_000545.8(HNF1A):c.1460G>A (p.Ser487Asn)	rs2464196	0.26206
NM_000545.8(HNF1A):c.1375C>T (p.Leu459=)	rs2259820	0.26141
NM_000545.8(HNF1A):c.864G>C (p.Gly288=)	rs56348580	0.25042
NM_000545.8(HNF1A):c.1545G>A (p.Thr515=)	rs55834942	0.13864
NM_000545.8(HNF1A):c.293C>T (p.Ala98Val)	rs1800574	0.02065
NM_000545.8(HNF1A):c.326+6_326+10dup	rs56158114	0.00415
NM_000545.8(HNF1A):c.1425G>A (p.Pro475=)	rs145589373	0.00232
NM_000545.8(HNF1A):c.1377G>A (p.Leu459=)	rs118028009	0.00020
NM_000545.8(HNF1A):c.1500C>T (p.His500=)	rs201694197	0.00017
NM_000545.8(HNF1A):c.1624-19G>A	rs193922586	0.00011

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