rs768191104
This variant is located in the SLFN14 gene.
▶ClinVar annotation
About SLFN14
The protein encoded by this gene plays an important role in platelet formation and function. Defects in this gene are a cause of thrombocytopenia with excessive bleeding. [provided by RefSeq, Jul 2016]
View all SLFN14 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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