Variant (rsID / SNP)

rs150687774

rs150687774 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ROGDI. Location: chromosome 16, position 4,848,579. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

ROGDIBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 16:4848579
Cytoband: 16p13.3
HGVS: NM_024589.3(ROGDI):c.522C>T (p.Ser174=)
Allele change: Synonymous_S174S

Associated conditions / phenotypes

Amelocerebrohypohidrotic syndrome

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.