ClinVar Miner

List of variants in gene PLA2G6 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 29
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_003560.4(PLA2G6):c.2340C>T (p.Asn780=) rs138683183 0.00691
NM_003560.4(PLA2G6):c.425+464C>T rs11570633 0.00512
NM_003560.4(PLA2G6):c.972G>A (p.Ala324=) rs147755372 0.00249
NM_003560.4(PLA2G6):c.990C>T (p.Phe330=) rs146241431 0.00167
NM_003560.4(PLA2G6):c.966C>T (p.His322=) rs144033740 0.00044
NM_003560.4(PLA2G6):c.101C>T (p.Ser34Leu) rs147948449 0.00040
NM_003560.4(PLA2G6):c.2417C>G (p.Pro806Arg) rs140758033 0.00021
NM_003560.4(PLA2G6):c.396C>T (p.Arg132=) rs146252218 0.00018
NM_003560.4(PLA2G6):c.1427C>T (p.Thr476Ile) rs146684391 0.00017
NM_003560.4(PLA2G6):c.564C>T (p.Thr188=) rs185396488 0.00016
NM_003560.4(PLA2G6):c.2259C>T (p.Val753=) rs749966284 0.00014
NM_003560.4(PLA2G6):c.447C>T (p.Asn149=) rs368631309 0.00011
NM_003560.4(PLA2G6):c.1725G>A (p.Thr575=) rs200599704 0.00010
NM_003560.4(PLA2G6):c.1614C>T (p.Arg538=) rs373930150 0.00007
NM_003560.4(PLA2G6):c.2355C>T (p.Thr785=) rs146591896 0.00005
NM_003560.4(PLA2G6):c.898G>A (p.Ala300Thr) rs528966598 0.00004
NM_003560.4(PLA2G6):c.1548G>A (p.Ala516=) rs1031583350 0.00003
NM_003560.4(PLA2G6):c.1779G>A (p.Pro593=) rs746984683 0.00002
NM_003560.4(PLA2G6):c.2277-7C>T rs571223704 0.00002
NM_003560.4(PLA2G6):c.858C>T (p.Tyr286=) rs756418076 0.00002
NM_003560.4(PLA2G6):c.948G>A (p.Ala316=) rs747199329 0.00002
NM_003560.4(PLA2G6):c.624C>T (p.Asn208=) rs536593896 0.00001
NM_003560.4(PLA2G6):c.1029G>A (p.Ala343=)
NM_003560.4(PLA2G6):c.102G>A (p.Ser34=)
NM_003560.4(PLA2G6):c.1200G>A (p.Lys400=) rs2145748343
NM_003560.4(PLA2G6):c.1890G>C (p.Val630=)
NM_003560.4(PLA2G6):c.1894C>A (p.Arg632=)
NM_003560.4(PLA2G6):c.2035-870C>A
NM_003560.4(PLA2G6):c.348C>T (p.Asn116=)

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.