ClinVar Miner

List of variants in gene combination SPRY3, TMLHE reported as risk factor for autism, susceptiblity to

Included ClinVar conditions (22):

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: 1

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HGVS	dbSNP	gnomAD frequency
NC_000023.11:g.(155524633_155545096)_(155545276_155612791)del

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