Variant (rsID / SNP)

rs3752362

rs3752362 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRKX. Location: chromosome X, position 3,631,167. The table records no clinical significance for this variant.

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Reference-table entries

PRKXNot classified

Variant type: missense_variant
Chromosome / position: X:3631167
HGVS: NM_005044.5,c.128T>C,p.Val43Ala
Allele change: Missense_V43A

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.