List of variants in gene combination KLF11, LOC128897170 reported as uncertain significance for disorder of glycolysis

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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: 8

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HGVS	dbSNP	gnomAD frequency
NM_003597.5(KLF11):c.-76G>A	rs1038766626	0.00583
NM_003597.5(KLF11):c.-83G>A	rs943136426	0.00055
NM_003597.5(KLF11):c.-104C>T	rs886054718	0.00038
NM_003597.5(KLF11):c.-146C>T	rs886054717	0.00033
NM_003597.5(KLF11):c.-108G>A	rs868540286	0.00015
NM_003597.5(KLF11):c.-159G>A	rs1445533585	0.00003
NM_003597.5(KLF11):c.-31G>A	rs886054721	0.00001
NM_003597.5(KLF11):c.-95GCC[7]	rs372827624

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