rs779452951

This variant is located in the SLC1A4 gene.

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ClinVar annotation

Uncertain Significance★☆☆☆

1 submitter1 publication

About SLC1A4

The protein encoded by this gene is a sodium-dependent neutral amino acid transporter for alanine, serine, cysteine, and threonine. Defects in this gene have been associated with developmental delay, microcephaly, and intellectual disability. [provided by RefSeq, Jan 2017]

View all SLC1A4 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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