RS121918732 TGM1

Health Risk Chr 14:24260554 snv missense variant
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What This Variant Does
"[OMIM:?]
Associated Conditions
Autosomal recessive congenital ichthyosis 1
Congenital ichthyosiform erythroderma
Lamellar ichthyosis
Autosomal recessive congenital ichthyosis 1
Congenital ichthyosiform erythroderma
Lamellar ichthyosis
Population Frequencies
gnomAD ALL
0%
Other Variants in TGM1
rs2139023508 rs41295338 rs121918719 rs121918728 rs121918716 rs121918717 rs121918718 rs121918720 rs121918721 rs121918722
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