List of variants in gene combination KCNN2, LOC101927078 reported by Institute for Human Genetics, University Hospital Essen

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_021614.4(KCNN2):c.1713T>G (p.Ile571Met)	rs1761282406
NM_021614.4(KCNN2):c.1718A>G (p.Tyr573Cys)	rs1761282515
NM_021614.4(KCNN2):c.1720G>A (p.Gly574Ser)	rs1761282724
NM_021614.4(KCNN2):c.1798C>G (p.Leu600Val)	rs1761822790
NM_021614.4(KCNN2):c.1890+2T>C	rs1761825165
NM_021614.4(KCNN2):c.1931T>C (p.Leu644Pro)	rs1747594790

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