ClinVar Miner

List of variants reported as benign for obsolete rare genetic deafness by Mendelics

Included ClinVar conditions (7):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_172095.4(CATSPER2):c.1179-2A>T	rs7169097	0.39868
NM_172095.4(CATSPER2):c.1179-3A>C	rs199882327	0.39865

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