List of variants in gene HNF1A reported as likely benign for benign neoplasm

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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: 16

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HGVS	dbSNP	gnomAD frequency
NM_000545.8(HNF1A):c.326+6_326+10dup	rs56158114	0.00415
NM_000545.8(HNF1A):c.1446C>T (p.Ser482=)	rs147366495	0.00117
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.1386C>T (p.Val462=)	rs143015301	0.00021
NM_000545.8(HNF1A):c.1108-4G>A	rs372892932	0.00020
NM_000545.8(HNF1A):c.1377G>A (p.Leu459=)	rs118028009	0.00020
NM_000545.8(HNF1A):c.1071G>A (p.Glu357=)	rs376279459	0.00006
NM_000545.8(HNF1A):c.1015G>A (p.Gly339Ser)	rs766790596	0.00004
NM_000545.8(HNF1A):c.150C>T (p.Cys50=)	rs193922583	0.00004
NM_000545.8(HNF1A):c.713+13G>A	rs755961371	0.00004
NM_000545.8(HNF1A):c.153C>T (p.Gly51=)	rs761779651	0.00001
NM_000545.8(HNF1A):c.685C>A (p.Arg229=)	rs769086289	0.00001
NM_000545.8(HNF1A):c.-167TGGGGGT[3]	rs538476099
NM_000545.8(HNF1A):c.1719_1720inv (p.Ser574Gly)
NM_000545.8(HNF1A):c.498C>T (p.Tyr166=)	rs1876675633

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