Variant (rsID / SNP)

rs7945121

rs7945121 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC22A24. Location: chromosome 11, position 62,847,453. The table records no clinical significance for this variant.

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Reference-table entries

SLC22A24Not classified

Variant type: missense_variant
Chromosome / position: 11:62847453
HGVS: NM_001136506.2,c.1618A>G,p.Ile540Val
Allele change: Missense_I540V

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.