Variant (rsID / SNP)

rs3803767

rs3803767 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC38A10. Location: chromosome 17, position 79,226,362. The table records no clinical significance for this variant.

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Reference-table entries

SLC38A10Not classified

Variant type: synonymous_variant
Chromosome / position: 17:79226362
HGVS: NM_001037984.3,c.1578C>T,p.His526His
Allele change: Synonymous_H526H

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.