RS1064793129 FOXN1

Health Risk Chr 17:28534759
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What This Variant Does
"CLNSIG=4
Associated Conditions
T-cell immunodeficiency
congenital alopecia
and nail dystrophy
T-cell lymphopenia
infantile
with or without nail dystrophy
autosomal dominant
T-cell immunodeficiency
congenital alopecia
and nail dystrophy
T-cell lymphopenia
infantile
with or without nail dystrophy
autosomal dominant
Other Variants in FOXN1
rs104894562 rs886043619 rs185748978 rs62640040 rs137872361 rs367793349 rs202144980 rs1057524466 rs1064796115 rs1064795660
Ask Dr. Hemsworth about this variant