List of variants in gene ADAR, LOC129931512 studied for autosomal recessive disease

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: 19

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001111.5(ADAR):c.15+10G>T	rs58655370	0.27999
NM_001111.5(ADAR):c.15+9G>A	rs749243606	0.00004
NM_001111.5(ADAR):c.15+16C>T	rs1353298437	0.00001
NM_001111.5(ADAR):c.15+20G>A	rs1269610582	0.00001
NM_001111.5(ADAR):c.11G>C (p.Arg4Pro)
NM_001111.5(ADAR):c.12G>T (p.Arg4=)
NM_001111.5(ADAR):c.14A>G (p.Gln5Arg)
NM_001111.5(ADAR):c.15+10G>A	rs58655370
NM_001111.5(ADAR):c.15+13G>C	rs1206051413
NM_001111.5(ADAR):c.15+15C>A
NM_001111.5(ADAR):c.15+15C>T
NM_001111.5(ADAR):c.15+4A>G	rs2101670089
NM_001111.5(ADAR):c.15+6C>G
NM_001111.5(ADAR):c.15+6C>T	rs1698312357
NM_001111.5(ADAR):c.15+7C>T
NM_001111.5(ADAR):c.15+8G>A
NM_001111.5(ADAR):c.1A>G (p.Met1Val)	rs1698314927
NM_001111.5(ADAR):c.7C>G (p.Pro3Ala)	rs1313399962
NM_001111.5(ADAR):c.7C>T (p.Pro3Ser)	rs1313399962

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.