Variant (rsID / SNP)

rs2252505

rs2252505 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ATPSCKMT. Location: chromosome 5, position 10,239,278. The table records no clinical significance for this variant.

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Reference-table entries

ATPSCKMTNot classified

Variant type: synonymous_variant
Chromosome / position: 5:10239278
HGVS: NM_199133.4,c.207G>A,p.Pro69Pro
Allele change: Synonymous_P69P

Associated conditions / phenotypes

Silent

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.