Variant (rsID / SNP)

rs9960464

rs9960464 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC14A2. Location: chromosome 18, position 43,246,156. The table records no clinical significance for this variant.

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Reference-table entries

SLC14A2Not classified

Variant type: missense_variant
Chromosome / position: 18:43246156
HGVS: NM_001242692.2,c.1529G>A,p.Arg510Gln
Allele change: Missense_R510Q

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.