List of variants in gene combination RELN, SLC26A5 reported as uncertain significance by Fulgent Genetics, Fulgent Genetics

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_005045.4(RELN):c.8843+3A>C	rs200124755	0.00029
NM_005045.4(RELN):c.8212C>T (p.Arg2738Trp)	rs202166176	0.00016
NM_005045.4(RELN):c.8795C>A (p.Ser2932Tyr)	rs139225791	0.00014
NM_005045.4(RELN):c.9329G>A (p.Arg3110Gln)	rs368572382	0.00014
NM_005045.4(RELN):c.10322G>A (p.Arg3441Gln)	rs116463039	0.00011
NM_005045.4(RELN):c.10310T>C (p.Met3437Thr)	rs377638585	0.00007
NM_005045.4(RELN):c.10357C>T (p.Arg3453Ter)	rs139326865	0.00006
NM_005045.4(RELN):c.8624C>T (p.Pro2875Leu)	rs761738403	0.00003
NM_005045.4(RELN):c.10025C>T (p.Thr3342Met)	rs201703640	0.00002
NM_005045.4(RELN):c.8213G>A (p.Arg2738Gln)	rs141115137

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