Variant (rsID / SNP)

rs61935924

rs61935924 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RXYLT1. Location: chromosome 12, position 64,173,807. Clinical significance in the table: Benign.

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Reference-table entries

RXYLT1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 12:64173807
Cytoband: 12q14.2
HGVS: NM_014254.3(RXYLT1):c.67G>A (p.Ala23Thr)
Allele change: Missense_A23T

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.