List of variants in gene ARSL reported as uncertain significance for X-linked chondrodysplasia punctata 1

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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: 8

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HGVS	dbSNP
NM_000047.2(ARSL):c.1239C>A (p.Asp413Glu)	rs142382411
NM_000047.2(ARSL):c.1694T>G (p.Ile565Ser)	rs142375403
NM_000047.2(ARSL):c.36G>C (p.Arg12Ser)	rs122460151
NM_000047.2(ARSL):c.970G>A (p.Glu324Lys)	rs1555909467
NM_000047.3(ARSL):c.1022G>T (p.Gly341Val)	rs0
NM_000047.3(ARSL):c.512A>G (p.Tyr171Cys)	rs0
NM_000047.3(ARSL):c.684C>G (p.Ile228Met)	rs1359359899
NM_000047.3(ARSL):c.898G>A (p.Val300Ile)	rs752354785

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