List of variants in gene ARL6IP1 reported as uncertain significance for Hereditary spastic paraplegia 61

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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: 15

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HGVS	dbSNP	gnomAD frequency
NM_015161.3(ARL6IP1):c.490A>C (p.Ile164Leu)	rs200377377	0.00019
NM_015161.3(ARL6IP1):c.347G>A (p.Arg116Gln)	rs189570291	0.00003
NM_015161.3(ARL6IP1):c.493+5G>A	rs756391857	0.00002
NM_015161.3(ARL6IP1):c.113G>A (p.Arg38Gln)	rs375463688	0.00001
NM_015161.3(ARL6IP1):c.171G>A (p.Leu57=)	rs767572069	0.00001
NM_015161.3(ARL6IP1):c.205G>A (p.Gly69Ser)	rs770346896	0.00001
NM_015161.3(ARL6IP1):c.263C>T (p.Ala88Val)	rs374401441	0.00001
NM_015161.3(ARL6IP1):c.433C>G (p.Leu145Val)	rs781061128	0.00001
NM_015161.3(ARL6IP1):c.440C>T (p.Ala147Val)	rs1461337328	0.00001
NM_015161.3(ARL6IP1):c.566G>A (p.Arg189Lys)	rs148872516	0.00001
NM_015161.3(ARL6IP1):c.190C>G (p.Pro64Ala)	rs2506669232
NM_015161.3(ARL6IP1):c.260T>C (p.Leu87Pro)	rs2506668918
NM_015161.3(ARL6IP1):c.324T>G (p.Ile108Met)	rs2506661608
NM_015161.3(ARL6IP1):c.391G>A (p.Glu131Lys)	rs2506661231
NM_015161.3(ARL6IP1):c.408+4C>G	rs1596945553

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