List of variants reported as uncertain significance for pancreas disorder by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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Total variants: 30

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HGVS	dbSNP	gnomAD frequency
NM_000209.4(PDX1):c.-18C>T	rs193922351	0.00540
NM_000162.5(GCK):c.46-12C>T	rs142829768	0.00296
NM_000458.4(HNF1B):c.1045+12T>C	rs141166864	0.00097
NM_175914.5(HNF4A):c.426+6G>A	rs182980547	0.00070
NM_175914.5(HNF4A):c.826+30dup	rs193922478	0.00031
NM_000352.6(ABCC8):c.4412-14C>T	rs193922404	0.00016
NM_000545.8(HNF1A):c.1624-19G>A	rs193922586	0.00011
NM_000545.8(HNF1A):c.954C>T (p.His318=)	rs193922607	0.00006
NM_000458.4(HNF1B):c.1654-4G>A	rs193922485	0.00005
NM_000352.6(ABCC8):c.2117-12C>A	rs193922398	0.00004
NM_000545.8(HNF1A):c.1310-12C>T	rs193922579	0.00004
NM_000545.8(HNF1A):c.1624-15G>A	rs193922585	0.00004
NM_000162.5(GCK):c.-5T>C	rs193922251	0.00001
NM_000545.8(HNF1A):c.713+14C>T	rs193922601	0.00001
GCK:c.864-159_864-149del	rs386134235
NM_000162.5(GCK):c.1019+16G>A	rs193922256
NM_000162.5(GCK):c.208+9T>A	rs193922288
NM_000162.5(GCK):c.364-41dup	rs193922293
NM_000162.5(GCK):c.364-49dup	rs193922294
NM_000162.5(GCK):c.45+11C>G	rs193922298
NM_000162.5(GCK):c.680-94dup	rs193922321
NM_000162.5(GCK):c.863+3A>G	rs193922334
NM_000209.4(PDX1):c.-50CTCCCGG[5]	rs193922352
NM_000209.4(PDX1):c.714GCC[6] (p.Pro244_Gly245insPro)	rs193922357
NM_000352.6(ABCC8):c.1332+17G>C	rs193922395
NM_000458.4(HNF1B):c.-14dup	rs193922481
NM_000458.4(HNF1B):c.1654-11_1654-9delinsC	rs386134268
NM_000492.4(CFTR):c.3718-2473_3718-2472insCAGAGT	rs397515289
NM_000545.8(HNF1A):c.1768+65dup	rs193922590
NM_000545.8(HNF1A):c.326+4A>G	rs193922595

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