RS138125827 CHRNG

Health Risk Chr 2:232543051 snv missense variant
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Associated Conditions
Autosomal recessive multiple pterygium syndrome
Lethal multiple pterygium syndrome
Autosomal recessive multiple pterygium syndrome
Lethal multiple pterygium syndrome
Population Frequencies
gnomAD ALL
0%
1kG AFR
0.4%
1kG ALL
0.1%
1kG AMR
100%
1kG EAS
100%
1kG EUR
100%
1kG SAS
100%
Other Variants in CHRNG
rs267606725 rs121912670 rs121912671 rs267606726 rs121912672 rs767503038 rs786205549 rs797044677 rs773463683 rs765746795
Ask Dr. Hemsworth about this variant