Variant (rsID / SNP)

rs34461862

rs34461862 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC14A2. Location: chromosome 18, position 43,204,739. The table records no clinical significance for this variant.

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Reference-table entries

SLC14A2Not classified

Variant type: missense_variant
Chromosome / position: 18:43204739
HGVS: NM_001242692.2,c.110C>T,p.Thr37Ile
Allele change: Missense_T37I

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.