List of variants in gene HNF1A reported as benign by Athena Diagnostics Inc

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)
		ClinVar version:

Total variants: 28

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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+20C>A	rs80051981	0.00772
NM_000545.8(HNF1A):c.326+6_326+10dup	rs56158114	0.00415
NM_000545.8(HNF1A):c.276C>T (p.Leu92=)	rs34056805	0.00269
NM_000545.8(HNF1A):c.1425G>A (p.Pro475=)	rs145589373	0.00232
NM_000545.8(HNF1A):c.252C>T (p.Pro84=)	rs78772552	0.00215
NM_000545.8(HNF1A):c.1165T>G (p.Leu389Val)	rs115080759	0.00198
NM_000545.8(HNF1A):c.1704C>T (p.Pro568=)	rs148520816	0.00103
NM_000545.8(HNF1A):c.1722C>A (p.Ser574Arg)	rs141304623	0.00103
NM_000545.8(HNF1A):c.1107+9C>G	rs17847497	0.00081
NM_000545.8(HNF1A):c.1323G>A (p.Thr441=)	rs138996307	0.00081
NM_000545.8(HNF1A):c.92G>A (p.Gly31Asp)	rs137853247	0.00076
NM_000545.8(HNF1A):c.210C>T (p.Ser70=)	rs146686581	0.00061
NM_000545.8(HNF1A):c.1502-7C>T	rs193922581	0.00046
NM_000545.8(HNF1A):c.1539C>T (p.Thr513=)	rs193922584	0.00037
NM_000545.8(HNF1A):c.336G>A (p.Pro112=)	rs371365341	0.00036
NM_000545.8(HNF1A):c.1500C>T (p.His500=)	rs201694197	0.00017
NM_000545.8(HNF1A):c.1624-19G>A	rs193922586	0.00011
NM_000545.8(HNF1A):c.871C>T (p.Pro291Ser)	rs151256267	0.00006
NM_000545.8(HNF1A):c.1310-12C>T	rs193922579	0.00004
NM_000545.8(HNF1A):c.-4A>G	rs561269721	0.00001

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