List of variants in gene ABCC8 reported as not provided

Minimum submission review status:		Collection method:
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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: 14

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HGVS	dbSNP	gnomAD frequency
NM_000352.6(ABCC8):c.1144G>A (p.Glu382Lys)	rs80356651
NM_000352.6(ABCC8):c.2147G>T (p.Gly716Val)	rs72559723
NM_000352.6(ABCC8):c.215A>G (p.Asn72Ser)	rs80356634
NM_000352.6(ABCC8):c.257T>C (p.Val86Ala)	rs193929360
NM_000352.6(ABCC8):c.257T>G (p.Val86Gly)	rs193929360
NM_000352.6(ABCC8):c.3554C>A (p.Ser1185Tyr)	rs193929369
NM_000352.6(ABCC8):c.394T>C (p.Phe132Leu)	rs80356637
NM_000352.6(ABCC8):c.394T>G (p.Phe132Val)	rs80356637
NM_000352.6(ABCC8):c.404T>C (p.Leu135Pro)	rs193929364
NM_000352.6(ABCC8):c.4270A>G (p.Ile1424Val)	rs80356653
NM_000352.6(ABCC8):c.627C>A (p.Asp209Glu)	rs80356640
NM_000352.6(ABCC8):c.631C>A (p.Gln211Lys)	rs193929366
NM_000352.6(ABCC8):c.638T>G (p.Leu213Arg)	rs80356642
NM_000352.6(ABCC8):c.674T>C (p.Leu225Pro)	rs1048095

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