List of variants in gene combination FLVCR1, LOC129932486 reported as uncertain significance for autosomal recessive degenerative and progressive 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_014053.4(FLVCR1):c.241C>T (p.Leu81=)	rs1251133617	0.00001
NM_014053.4(FLVCR1):c.82G>A (p.Gly28Ser)	rs746296931	0.00001
NM_014053.4(FLVCR1):c.236C>T (p.Ala79Val)	rs767746826
NM_014053.4(FLVCR1):c.270C>A (p.Thr90=)	rs534403116

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