List of variants in gene KCNH2 studied for SUDDEN INFANT DEATH SYNDROME

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: 7

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000238.4(KCNH2):c.2684C>T (p.Thr895Met)	rs199473434	0.00005
NM_000238.4(KCNH2):c.2860C>T (p.Arg954Cys)	rs141401803	0.00004
NM_000238.4(KCNH2):c.3470C>T (p.Pro1157Leu)	rs143167166	0.00003
NM_000238.4(KCNH2):c.3118A>G (p.Ser1040Gly)	rs199473024	0.00001
NM_000238.4(KCNH2):c.818G>A (p.Arg273Gln)	rs199472877
NM_000238.4(KCNH2):c.835G>A (p.Val279Met)	rs199472879
NM_000238.4(KCNH2):c.881G>T (p.Gly294Val)	rs199473549

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.