ClinVar Miner

List of variants in gene combination CFAP126, SDHC reported by Quest Diagnostics Nichols Institute San Juan Capistrano

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
GRCh37/hg19 1q23.3(chr1:161299064-161414959)x3
GRCh37/hg19 1q23.3(chr1:161333248-161380335)x1
NM_003001.3(SDHC):c.406-408_*4225del

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