Variant (rsID / SNP)

rs138846036

rs138846036 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HGD. Location: chromosome 3, position 120,393,782. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

HGDBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 3:120393782
Cytoband: 3q13.33
HGVS: NM_000187.4(HGD):c.142G>T (p.Ala48Ser)
Allele change: Missense_A48S

Associated conditions / phenotypes

Alkaptonuria

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.