ClinVar Miner

List of variants in gene LRRC32 studied for cleft palate, proliferative retinopathy, and developmental delay

Included ClinVar conditions (1):

Cleft palate, proliferative retinopathy, and developmental delay

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001128922.2(LRRC32):c.1630C>T (p.Arg544Ter)	rs369867819
NM_001128922.2(LRRC32):c.980T>C (p.Ile327Thr)	rs2120049760
NM_001370189.1(LRRC32):c.9C>A (p.Cys3Ter)	rs1251757869

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