List of variants in gene FBXO38 reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_205836.3(FBXO38):c.2146A>G (p.Ser716Gly)	rs150893158	0.00048
NM_205836.3(FBXO38):c.1117G>A (p.Val373Met)	rs201279960	0.00011
NM_205836.3(FBXO38):c.2683A>G (p.Met895Val)	rs758909222	0.00006
NM_205836.3(FBXO38):c.1609G>C (p.Ala537Pro)	rs1460688537	0.00001
NM_205836.3(FBXO38):c.373G>A (p.Ala125Thr)
NM_205836.3(FBXO38):c.61A>G (p.Met21Val)	rs1581225783
NM_205836.3(FBXO38):c.712G>C (p.Val238Leu)	rs144890577

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