Variant (rsID / SNP)

rs7827446

rs7827446 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PXDNL. Location: chromosome 8, position 52,233,408. The table records no clinical significance for this variant.

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Reference-table entries

PXDNLNot classified

Variant type: missense_variant
Chromosome / position: 8:52233408
HGVS: NM_144651.5,c.4196G>A,p.Arg1399Lys
Allele change: Missense_R1399K

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.