RS797044677 CHRNG

Health Risk Chr 2:232540049
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Autosomal recessive multiple pterygium syndrome
Lethal multiple pterygium syndrome
Inborn genetic diseases
Autosomal recessive multiple pterygium syndrome
Lethal multiple pterygium syndrome
Other Variants in CHRNG
rs267606725 rs121912670 rs121912671 rs267606726 rs121912672 rs767503038 rs786205549 rs138125827 rs773463683 rs765746795
Ask Dr. Hemsworth about this variant