Variant (rsID / SNP)

rs2245220

rs2245220 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRND. Location: chromosome 20, position 4,705,718. The table records no clinical significance for this variant.

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Reference-table entries

PRNDNot classified

Variant type: missense_variant
Chromosome / position: 20:4705718
HGVS: NM_012409.4,c.521C>T,p.Thr174Met
Allele change: Missense_T174M

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.