List of variants in gene KIRREL3 reported as uncertain significance by Genetic Services Laboratory, University of Chicago

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_032531.4(KIRREL3):c.396C>T (p.Ala132=)	rs35152573	0.00069
NM_032531.4(KIRREL3):c.1395G>A (p.Ser465=)	rs138978113	0.00040
NM_032531.4(KIRREL3):c.207C>T (p.Cys69=)	rs371273662	0.00002
NM_032531.4(KIRREL3):c.1195C>T (p.Arg399Trp)	rs1242650611	0.00001
NM_032531.4(KIRREL3):c.1354-6G>C	rs587780376	0.00001
NM_032531.4(KIRREL3):c.1991C>T (p.Ala664Val)	rs200640353	0.00001
NM_032531.4(KIRREL3):c.327G>A (p.Glu109=)	rs547399629	0.00001
NM_032531.4(KIRREL3):c.103G>A (p.Ala35Thr)	rs549320678
NM_032531.4(KIRREL3):c.1217G>A (p.Gly406Glu)	rs1955736095
NM_032531.4(KIRREL3):c.655G>A (p.Val219Met)	rs200789628
NM_032531.4(KIRREL3):c.669G>A (p.Gln223=)	rs1473256132

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