List of variants in gene combination LOC130065680, SNTA1 studied for Long QT syndrome 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: 16

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_003098.2(SNTA1):c.-255G>C	rs57684257	0.08518
NM_003098.3(SNTA1):c.-96G>A	rs145471317	0.01886
NM_003098.2(SNTA1):c.-245C>A	rs531929083	0.00728
NM_003098.3(SNTA1):c.128G>A (p.Ser43Asn)	rs786205841	0.00022
NM_003098.3(SNTA1):c.40G>A (p.Glu14Lys)	rs786205846	0.00014
NM_003098.3(SNTA1):c.-261C>A	rs536994978	0.00010
NM_003098.3(SNTA1):c.-262C>T	rs550104436	0.00010
NM_003098.3(SNTA1):c.101G>A (p.Ser34Asn)	rs963277918	0.00009
NM_003098.3(SNTA1):c.25C>T (p.Arg9Cys)	rs886039012	0.00002
NM_003098.3(SNTA1):c.-18G>A	rs886056628	0.00001
NM_003098.3(SNTA1):c.-42G>A	rs921708182	0.00001
NM_003098.3(SNTA1):c.115G>A (p.Val39Met)	rs755986911	0.00001
NM_003098.2(SNTA1):c.-186C>T	rs886056629
NM_003098.3(SNTA1):c.-62C>T	rs1990639431
NM_003098.3(SNTA1):c.-70C>A	rs930437100
NM_003098.3(SNTA1):c.-96G>C	rs145471317

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.