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Variant (rsID / SNP)

rs664370

PXT1

rs664370 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PXT1. Location: chromosome 6, position 36,393,816. The table records no clinical significance for this variant.

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Reference-table entries

PXT1Not classified
Variant type
missense_variant
Chromosome / position
6:36393816
HGVS
NM_152990.4,c.44T>C,p.Val15Ala
Allele change
Missense_V15A

Public references

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