FAM47C Chromosome X

Family with sequence similarity 47 member C
2 variants 2 Health Risk

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What This Gene Does
This gene encodes a product belonging to a family of proteins with unknown function. The coding sequence of this family member includes several tandemly repeated regions. [provided by RefSeq, Sep 2011]
Key Variants
All Variants (2)
RSID Category Clinical Significance Conditions
RS148624854 Health Risk Conflicting classifications of pathogenicity
RS199727942 Health Risk Conflicting classifications of pathogenicity
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