RS767503038 CHRNG

Health Risk Chr 2:232543030
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What This Variant Does
"CLNSIG=5
Associated Conditions
Lethal multiple pterygium syndrome
Autosomal recessive multiple pterygium syndrome
Inborn genetic diseases
CHRNG-related disorder
Abnormality of prenatal development or birth
Lethal multiple pterygium syndrome
Autosomal recessive multiple pterygium syndrome
Inborn genetic diseases
CHRNG-related disorder
Abnormality of prenatal development or birth
Other Variants in CHRNG
rs267606725 rs121912670 rs121912671 rs267606726 rs121912672 rs786205549 rs797044677 rs138125827 rs773463683 rs765746795
Ask Dr. Hemsworth about this variant