Variant (rsID / SNP)

rs61732365

rs61732365 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC22A31. Location: chromosome 16, position 89,265,087. The table records no clinical significance for this variant.

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Reference-table entries

SLC22A31Not classified

Variant type: missense_variant
Chromosome / position: 16:89265087
HGVS: NM_001384763.1,c.571T>C,p.Ser191Pro
Allele change: Missense_S83P

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.