List of variants in gene combination LOC101928008, SBF2 reported as uncertain significance by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_030962.4(SBF2):c.3290C>A (p.Thr1097Asn)	rs141894081	0.00054
NM_030962.4(SBF2):c.3433A>G (p.Arg1145Gly)	rs145647154	0.00023
NM_030962.4(SBF2):c.1967G>C (p.Cys656Ser)	rs138120231	0.00019
NM_030962.4(SBF2):c.2197C>G (p.Gln733Glu)	rs145199888	0.00014
NM_030962.4(SBF2):c.3163A>G (p.Ile1055Val)	rs142891020	0.00004
NM_030962.4(SBF2):c.2894A>G (p.Asn965Ser)	rs1008248276

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