List of variants in gene combination C12orf43, HNF1A reported as benign for pancreas disorder

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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: 28

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HGVS	dbSNP	gnomAD frequency
NM_000545.8(HNF1A):c.*438G>A	rs1169310	0.30485
NM_000545.8(HNF1A):c.*197G>T	rs1169309	0.30438
NM_000545.8(HNF1A):c.*1268G>A	rs41279096	0.11781
NM_000545.8(HNF1A):c.*603G>A	rs11065390	0.05950
NM_000545.8(HNF1A):c.*214G>A	rs191295371	0.00327
NM_000545.8(HNF1A):c.*908G>A	rs140584786	0.00236
NM_000545.8(HNF1A):c.*939G>A	rs751401246	0.00054
NM_000545.8(HNF1A):c.*1070C>T	rs568653423	0.00046
NM_000545.8(HNF1A):c.*1312C>T	rs56335342	0.00045
NM_000545.8(HNF1A):c.*1044G>A	rs1039799815	0.00028
NM_000545.8(HNF1A):c.*170C>T	rs547080919	0.00022
NM_000545.8(HNF1A):c.*1165C>T	rs927067298	0.00020
NM_000545.8(HNF1A):c.*447T>A	rs143731661	0.00019
NM_000545.8(HNF1A):c.*864C>T	rs750496742	0.00014
NM_000545.8(HNF1A):c.*621C>T	rs1026422272	0.00013
NM_000545.8(HNF1A):c.*865G>A	rs571134960	0.00011
NM_000545.8(HNF1A):c.1849G>A (p.Val617Ile)	rs146855738	0.00006
NM_000545.8(HNF1A):c.1816G>A (p.Gly606Ser)	rs753972576	0.00005
NM_000545.8(HNF1A):c.*1090T>C	rs1045819255	0.00001
NM_000545.8(HNF1A):c.1780A>G (p.Ser594Gly)	rs751112023	0.00001
NM_000545.8(HNF1A):c.1800C>T (p.Ser600=)	rs756416683	0.00001
NM_000545.8(HNF1A):c.*1071G>A	rs886049035
NM_000545.8(HNF1A):c.*193C>T	rs972789249
NM_000545.8(HNF1A):c.*196G>A	rs1877471070
NM_000545.8(HNF1A):c.*267T>G	rs571084139
NM_000545.8(HNF1A):c.*335C>T	rs1877483762
NM_000545.8(HNF1A):c.*39G>T	rs758414199
NM_000545.8(HNF1A):c.*589C>T	rs55962050

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