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Variant (rsID / SNP)

rs164365

SLC5A8

rs164365 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC5A8. Location: chromosome 12, position 101,560,328. The table records no clinical significance for this variant.

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Reference-table entries

SLC5A8Not classified
Variant type
missense_variant
Chromosome / position
12:101560328
HGVS
NM_145913.5,c.1470G>T,p.Met490Ile
Allele change
Missense_M490I

Associated conditions / phenotypes

Prostatic Hypertrophy|Prostatic Hyperplasia, Benign|Prostatic Adenoma

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.