ClinVar Miner

List of variants in gene KCNJ2, LOC130061539 studied for short QT syndrome

Included ClinVar conditions (12):

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
NM_000891.3(KCNJ2):c.-349C>A	rs370696463	0.00011
NM_000891.3(KCNJ2):c.-348G>A	rs993406508	0.00003
NM_000891.3(KCNJ2):c.-361G>C	rs984704301	0.00001

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