rs2532606875
This variant is located in the RHAG gene.
▶ClinVar annotation
Uncertain Significance★☆☆☆
1 submitter1 publicationAbout RHAG
The protein encoded by this gene is erythrocyte-specific and is thought to be part of a membrane channel that transports ammonium and carbon dioxide across the blood cell membrane. The encoded protein appears to interact with Rh blood group antigens and Rh30 polypeptides. Defects in this gene are a cause of regulator type Rh-null hemolytic anemia (RHN), or Rh-deficiency syndrome.[provided by RefSeq, Mar 2009]
View all RHAG variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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