List of variants in gene combination RELN, SLC26A5 reported as likely benign for Norman-Roberts syndrome

Minimum submission review status:		Collection method:
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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_005045.4(RELN):c.*576G>A	rs141550459	0.00484
NM_005045.4(RELN):c.9321C>T (p.Leu3107=)	rs150387973	0.00218
NM_005045.4(RELN):c.10093G>A (p.Val3365Ile)	rs115035120	0.00018
NM_005045.4(RELN):c.8863C>T (p.Arg2955Cys)	rs114501042	0.00018

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