ClinVar Miner

List of variants reported as benign for T-cell immunodeficiency, congenital alopecia, and nail dystrophy by Invitae

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 23
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001369369.1(FOXN1):c.124-20G>A rs614434 0.64317
NM_001369369.1(FOXN1):c.830+19A>G rs548973 0.43360
NM_001369369.1(FOXN1):c.1795G>C (p.Ala599Pro) rs532648 0.38842
NM_001369369.1(FOXN1):c.1135+8C>T rs2286521 0.15430
NM_001369369.1(FOXN1):c.852T>C (p.Leu284=) rs12449554 0.08836
NM_001369369.1(FOXN1):c.205C>T (p.Arg69Cys) rs2071587 0.07832
NM_001369369.1(FOXN1):c.1288C>T (p.Pro430Ser) rs61749867 0.03097
NM_001369369.1(FOXN1):c.714T>C (p.Gly238=) rs35240903 0.02200
NM_001369369.1(FOXN1):c.1425G>A (p.Pro475=) rs115771646 0.00591
NM_001369369.1(FOXN1):c.1215C>T (p.Ser405=) rs116778145 0.00572
NM_001369369.1(FOXN1):c.1710G>A (p.Ser570=) rs143371127 0.00399
NM_001369369.1(FOXN1):c.123+11G>A rs79946739 0.00344
NM_001369369.1(FOXN1):c.9G>A (p.Ser3=) rs146390262 0.00295
NM_001369369.1(FOXN1):c.550C>A (p.Leu184Ile) rs202144980 0.00264
NM_001369369.1(FOXN1):c.382C>T (p.Arg128Trp) rs144301161 0.00210
NM_001369369.1(FOXN1):c.321C>T (p.Ala107=) rs138295148 0.00197
NM_001369369.1(FOXN1):c.1131G>A (p.Lys377=) rs139218809 0.00132
NM_001369369.1(FOXN1):c.735C>T (p.Tyr245=) rs374130313 0.00031
NM_001369369.1(FOXN1):c.1664C>T (p.Ala555Val) rs187814037 0.00009
NM_001369369.1(FOXN1):c.279C>G (p.Leu93=) rs374082998 0.00004
NM_001369369.1(FOXN1):c.1443G>T (p.Leu481=) rs548817079
NM_001369369.1(FOXN1):c.162C>T (p.Asp54=) rs200786966
NM_001369369.1(FOXN1):c.362C>T (p.Ala121Val) rs557541901

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.