ClinVar Miner

List of variants in gene CCDST, FLG studied for Dermatitis, atopic, 2

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_002016.2(FLG):c.9947C>G (p.Ser3316Ter) rs149484917 0.00246
NM_002016.2(FLG):c.2476C>T (p.Arg826Ter) rs115746363 0.00243
NM_002016.2(FLG):c.9740C>A (p.Ser3247Ter) rs150597413 0.00144
NM_002016.2(FLG):c.7031C>G (p.Ser2344Ter) rs372754256 0.00015
NM_002016.2(FLG):c.7837A>T (p.Arg2613Ter) rs567795279 0.00010
NM_002016.2(FLG):c.10225C>T (p.Arg3409Ter) rs201356558 0.00003
NM_002016.2(FLG):c.7564C>T (p.Gln2522Ter) rs767261854 0.00001
NM_002016.2(FLG):c.10469_10471del (p.Arg3490_Asn3491delinsHis)
NM_002016.2(FLG):c.11684C>T (p.Ser3895Leu) rs2525130517
NM_002016.2(FLG):c.1501C>T (p.Arg501Ter) rs61816761
NM_002016.2(FLG):c.2282_2285del (p.Ser761fs) rs558269137
NM_002016.2(FLG):c.3222_3225del (p.Ser1074fs) rs745915174
NM_002016.2(FLG):c.4676C>A (p.Ser1559Ter) rs1446081294
NM_002016.2(FLG):c.5170G>T (p.Gly1724Ter) rs747301529
NM_002016.2(FLG):c.6395A>G (p.Gln2132Arg) rs1279861130
NM_002016.2(FLG):c.7339C>T (p.Arg2447Ter) rs138726443
NM_002016.2(FLG):c.7663G>T (p.Glu2555Ter) rs760728737
NM_002016.2(FLG):c.7777G>T (p.Gly2593Ter) rs756353784
NM_002016.2(FLG):c.9901A>T (p.Arg3301Ter) rs2525145486

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.