List of variants in gene combination FAT2, SLC36A1 reported as uncertain significance for cerebellar ataxia

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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: 17

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HGVS	dbSNP	gnomAD frequency
NM_001447.3(FAT2):c.12464C>G (p.Ser4155Cys)	rs145466001	0.00031
NM_001447.3(FAT2):c.10673G>A (p.Arg3558Gln)	rs137870998	0.00004
NM_001447.3(FAT2):c.12899T>C (p.Met4300Thr)	rs1443089616	0.00002
NM_001447.3(FAT2):c.10758G>C (p.Lys3586Asn)	rs770597316	0.00001
NM_001447.3(FAT2):c.10946G>A (p.Arg3649Gln)	rs201335279	0.00001
NM_001447.3(FAT2):c.11978C>T (p.Ala3993Val)	rs748005307	0.00001
NM_001447.3(FAT2):c.10111A>G (p.Ile3371Val)
NM_001447.3(FAT2):c.11435C>T (p.Thr3812Ile)
NM_001447.3(FAT2):c.11792C>T (p.Thr3931Met)
NM_001447.3(FAT2):c.12337A>G (p.Asn4113Asp)
NM_001447.3(FAT2):c.3781G>C (p.Gly1261Arg)
NM_001447.3(FAT2):c.5237T>C (p.Val1746Ala)	rs765754012
NM_001447.3(FAT2):c.5662G>A (p.Gly1888Ser)
NM_001447.3(FAT2):c.7018G>A (p.Glu2340Lys)
NM_001447.3(FAT2):c.7652G>A (p.Arg2551Lys)
NM_001447.3(FAT2):c.9835C>G (p.Leu3279Val)	rs1363769217
NM_001447.3(FAT2):c.9896C>T (p.Ser3299Phe)	rs2127588750

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