List of variants in gene RELN reported as likely pathogenic for epilepsy

Minimum submission review status:		Collection method:
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: 17

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HGVS	dbSNP	gnomAD frequency
NM_005045.4(RELN):c.3912+2T>G	rs1226957030	0.00001
NM_005045.4(RELN):c.7349+2T>C	rs982831716	0.00001
NC_000007.13:g.(?_103196019)_(103206706_?)del
NC_000007.14:g.(?_103589576)_(103610827_?)dup
NM_005045.4(RELN):c.2002+1G>A
NM_005045.4(RELN):c.2303+1G>A	rs2117350995
NM_005045.4(RELN):c.2303+2T>G
NM_005045.4(RELN):c.2465+2T>G
NM_005045.4(RELN):c.3463dup (p.Leu1155fs)	rs1831540987
NM_005045.4(RELN):c.473+1G>A
NM_005045.4(RELN):c.4936+1G>T
NM_005045.4(RELN):c.5615-2A>G	rs2117168257
NM_005045.4(RELN):c.6068_6072+20del
NM_005045.4(RELN):c.6314del (p.Phe2105fs)	rs1830269249
NM_005045.4(RELN):c.7180+1G>T	rs2117126444
NM_005045.4(RELN):c.805+1G>T
NM_005045.4(RELN):c.9453del (p.Trp3152fs)

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