List of variants in gene RELN reported as uncertain significance by Mayo Clinic Laboratories, Mayo Clinic

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_005045.4(RELN):c.5822T>C (p.Val1941Ala)	rs149837553	0.00041
NM_005045.4(RELN):c.5711C>T (p.Thr1904Met)	rs114190729	0.00025
NM_005045.4(RELN):c.6647G>A (p.Arg2216Gln)	rs200010849	0.00017
NM_005045.4(RELN):c.113T>A (p.Phe38Tyr)	rs149715692	0.00012
NM_005045.4(RELN):c.7590C>A (p.Asn2530Lys)	rs766869538	0.00004
NM_005045.4(RELN):c.7757C>T (p.Thr2586Ile)	rs202172902	0.00004
NM_005045.4(RELN):c.3412G>A (p.Gly1138Arg)	rs772114071	0.00001
NM_005045.4(RELN):c.2999A>G (p.Gln1000Arg)	rs772586514
NM_005045.4(RELN):c.3665A>T (p.Glu1222Val)	rs2117250095
NM_005045.4(RELN):c.457G>A (p.Gly153Ser)	rs2116408592
NM_005045.4(RELN):c.6595A>G (p.Ser2199Gly)

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