Variant (rsID / SNP)

rs1790218

rs1790218 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC22A10. Location: chromosome 11, position 63,057,925. The table records no clinical significance for this variant.

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Reference-table entries

SLC22A10Not classified

Variant type: stop_gained
Chromosome / position: 11:63057925
HGVS: NM_001039752.4,c.288G>A,p.Trp96*
Allele change: Silent

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.