Variant (rsID / SNP)

rs10493565

rs10493565 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC44A5. Location: chromosome 1, position 75,699,771. The table records no clinical significance for this variant.

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Reference-table entries

SLC44A5Not classified

Variant type: synonymous_variant
Chromosome / position: 1:75699771
HGVS: NM_152697.6,c.753T>C,p.Ile251Ile
Allele change: Synonymous_I251I

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.