ClinVar Miner

List of variants in gene ACTB, FBXL18, RBAK, RBAK-RBAKDN, SLC29A4, TNRC18, WIPI2 studied for Astigmatism; Autistic behavior; Myopia; Impaired social interactions; Aplasia/Hypoplasia of the inner ear

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: 1

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HGVS	dbSNP	gnomAD frequency
GRCh37/hg19 7p22.1(chr7:5096876-5569338)x1

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