List of variants reported as benign for autosomal dominant hyperinsulinism due to SUR1 deficiency by Illumina Laboratory Services, Illumina

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Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_000352.6(ABCC8):c.207T>C (p.Pro69=)	rs1048099	0.47531
NM_000352.6(ABCC8):c.579+14C>T	rs2301703	0.46493
NM_000352.6(ABCC8):c.1686C>T (p.His562=)	rs1799857	0.44260
NM_000352.6(ABCC8):c.2117-3C>T	rs1799854	0.36733
NM_000352.6(ABCC8):c.1947G>A (p.Lys649=)	rs1799858	0.16150
NM_000352.6(ABCC8):c.2485C>T (p.Leu829=)	rs1805036	0.14682
NM_000352.6(ABCC8):c.330C>T (p.Ala110=)	rs8192695	0.06691
NM_000352.6(ABCC8):c.-49G>C	rs77498130	0.03452
NM_000352.6(ABCC8):c.3612C>T (p.Ala1204=)	rs149861153	0.01269

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