List of variants in gene combination LOC101928008, SBF2 reported as likely benign for Charcot-Marie-Tooth disease type 4B2

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_030962.4(SBF2):c.2323G>A (p.Gly775Ser)	rs141330687	0.00267
NM_030962.4(SBF2):c.3036C>T (p.Thr1012=)	rs111967328	0.00167
NM_030962.4(SBF2):c.2337C>T (p.Ser779=)	rs140730386	0.00144
NM_030962.4(SBF2):c.2319G>A (p.Ala773=)	rs201547070	0.00016
NM_030962.4(SBF2):c.2436C>T (p.Ala812=)	rs374225152	0.00007
NM_030962.4(SBF2):c.1893C>T (p.Ala631=)	rs760154688	0.00001
NM_030962.4(SBF2):c.1863T>C (p.Asp621=)
NM_030962.4(SBF2):c.2611-35AATC[6]	rs202029370
NM_030962.4(SBF2):c.3292C>G (p.Leu1098Val)	rs117957652

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