ClinVar Miner

List of variants in gene CNTNAP2, LOC123956262, LOC129389920 studied for Pitt-Hopkins-like syndrome

Included ClinVar conditions (5):

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
GRCh38/hg38 7q35(chr7:146774271-146839904)x1
GRCh38/hg38 7q35(chr7:146774271-147132509)x1
NC_000007.13:g.(?_145813093)_(146537016_?)dup

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