Variant (rsID / SNP)

rs367035

rs367035 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC22A18. Location: chromosome 11, position 2,923,826. Clinical significance in the table: Benign.

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Reference-table entries

SLC22A18Benign

Clinical significance (as recorded): Benign
Variant type: start_lost
Chromosome / position: 11:2923826
HGVS: NM_001315501.2,c.1A>G,p.Met1?
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.