List of variants in gene RARS2, SLC35A1 studied for central nervous system malformation

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_006416.5(SLC35A1):c.*302A>G	rs1051131	0.61356
NM_006416.5(SLC35A1):c.*648T>G	rs1051148	0.61316
NM_020320.5(RARS2):c.1704A>G (p.Lys568=)	rs8802	0.12189
NM_006416.5(SLC35A1):c.887-14T>C	rs56136150	0.10768
NM_006416.5(SLC35A1):c.*147C>T	rs55960393	0.03465
NM_006416.5(SLC35A1):c.*240G>T	rs9450722	0.01462
NM_006416.5(SLC35A1):c.*294dup	rs11432150
NM_006416.5(SLC35A1):c.521_522insAATG	rs10681831

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