List of variants in gene ILDR1 reported as benign for not provided

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: 27

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HGVS	dbSNP	gnomAD frequency
NM_001199799.2(ILDR1):c.778+49G>A	rs3915060	0.75863
NM_001199799.2(ILDR1):c.1545T>G (p.Leu515=)	rs2877561	0.73781
NM_001199799.2(ILDR1):c.229+135T>C	rs11924058	0.65772
NM_001199799.2(ILDR1):c.791C>G (p.Pro264Arg)	rs3915061	0.31231
NM_001199799.2(ILDR1):c.1599+234C>T	rs12638492	0.21318
NM_001199799.2(ILDR1):c.1238T>C (p.Ile413Thr)	rs16832645	0.04001
NM_001199799.2(ILDR1):c.1325G>A (p.Arg442His)	rs34883204	0.03980
NM_001199799.2(ILDR1):c.1498C>T (p.His500Tyr)	rs34284625	0.03976
NM_001199799.2(ILDR1):c.778+37G>A	rs80084895	0.02284
NM_001199799.2(ILDR1):c.1298G>A (p.Arg433Gln)	rs35906279	0.02049
NM_001199799.2(ILDR1):c.1162T>C (p.Trp388Arg)	rs35661993	0.01612
NM_001199799.2(ILDR1):c.726G>A (p.Ala242=)	rs114464909	0.00814
NM_001199799.2(ILDR1):c.1581G>A (p.Gly527=)	rs142243054	0.00402
NM_001199799.2(ILDR1):c.764C>T (p.Pro255Leu)	rs144519399	0.00355
NM_001199799.2(ILDR1):c.1326C>A (p.Arg442=)	rs148350512	0.00282
NM_001199799.2(ILDR1):c.58+17T>C	rs112991162	0.00173
NM_001199799.2(ILDR1):c.1305C>A (p.Ser435Arg)	rs35597690	0.00120
NM_001199799.2(ILDR1):c.225A>G (p.Ser75=)	rs146402126	0.00098
NM_001199799.2(ILDR1):c.379+10G>C	rs200883040	0.00051
NM_001199799.2(ILDR1):c.1377C>T (p.His459=)	rs201105694	0.00027
NM_001199799.2(ILDR1):c.972C>T (p.Val324=)	rs138334785	0.00011
NM_001199799.2(ILDR1):c.792G>A (p.Pro264=)	rs186672543	0.00009
NM_001199799.2(ILDR1):c.380-117del	rs369348114
NM_001199799.2(ILDR1):c.380-155_380-147del	rs74268689
NM_001199799.2(ILDR1):c.426G>A (p.Val142=)
NM_001199799.2(ILDR1):c.499+77del	rs35657414
NM_001199799.2(ILDR1):c.499+98G>A	rs62269207

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