ClinVar Miner

List of variants in gene KCNJ1 reported by Fulgent Genetics, Fulgent Genetics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 19
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_153766.3(KCNJ1):c.252G>A (p.Ala84=) rs149563706 0.00576
NM_153766.3(KCNJ1):c.-21-2138C>T rs34191956 0.00071
NM_153766.3(KCNJ1):c.298A>G (p.Thr100Ala) rs138440917 0.00022
NM_153766.3(KCNJ1):c.1116G>A (p.Met372Ile) rs141900128 0.00015
NM_153766.3(KCNJ1):c.1034A>G (p.Asp345Gly) rs748305494 0.00011
NM_153766.3(KCNJ1):c.1019T>G (p.Leu340Arg) rs201176686 0.00008
NM_153766.3(KCNJ1):c.506G>A (p.Arg169His) rs759992526 0.00007
NM_153766.3(KCNJ1):c.34C>T (p.Arg12Cys) rs139738175 0.00004
NM_153766.3(KCNJ1):c.601C>T (p.Leu201Phe) rs200320892 0.00004
NM_153766.3(KCNJ1):c.272C>T (p.Pro91Leu) rs373745258 0.00003
NM_153766.3(KCNJ1):c.792G>A (p.Ala264=) rs567888166 0.00003
NM_153766.3(KCNJ1):c.842C>T (p.Thr281Ile) rs762988627 0.00003
NM_153766.3(KCNJ1):c.955C>T (p.Arg319Ter) rs377205432 0.00003
NM_153766.3(KCNJ1):c.-21-2122C>T rs111249880 0.00002
NM_153766.3(KCNJ1):c.584C>T (p.Ala195Val) rs104894246 0.00002
NM_153766.3(KCNJ1):c.242A>G (p.Tyr81Cys) rs387907439 0.00001
NM_153766.3(KCNJ1):c.867C>A (p.Cys289Ter) rs746509804 0.00001
NM_153766.3(KCNJ1):c.*1C>G
NM_153766.3(KCNJ1):c.578G>C (p.Arg193Pro) rs150299230

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.