List of variants in gene ILDR1 reported as uncertain significance for perceptual disorders

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_001199799.2(ILDR1):c.461C>T (p.Ser154Leu)	rs115649165	0.00057
NM_001199799.2(ILDR1):c.1297C>T (p.Arg433Trp)	rs140567004	0.00050
NM_001199799.2(ILDR1):c.1184T>C (p.Leu395Ser)	rs143311654	0.00037
NM_001199799.2(ILDR1):c.866T>G (p.Leu289Trp)	rs141450561	0.00023
NM_001199799.2(ILDR1):c.655C>T (p.Arg219Cys)	rs1365655840	0.00009
NM_001199799.2(ILDR1):c.1312C>T (p.Pro438Ser)	rs554966703	0.00008
NM_001199799.2(ILDR1):c.1291C>T (p.Arg431Cys)	rs376510686	0.00001
NM_001199799.2(ILDR1):c.182G>A (p.Arg61His)	rs138709949	0.00001
NM_001199799.2(ILDR1):c.1291_1305delinsGTGAGG (p.Arg431_Ser435delinsValArg)
NM_001199799.2(ILDR1):c.1301C>T (p.Pro434Leu)	rs760257421
NM_001199799.2(ILDR1):c.1358G>A (p.Arg453Gln)
NM_001199799.2(ILDR1):c.779-6A>G

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