rs140103005
This variant is located in the CFHR2 gene.
▶ClinVar annotation
Benign★★★☆
2 submitters1 publicationAbout CFHR2
This gene belongs to a family of complement factor H-related genes (CFHR), which are clustered together with complement factor H gene on chromosome 1, and are involved in regulation of complement. Mutations in CFHR genes have been associated with dense deposit disease and atypical haemolytic-uraemic syndrome. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Aug 2015]
View all CFHR2 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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