Variant (rsID / SNP)

rs3625

rs3625 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to JDP2. Location: chromosome 14, position 75,904,660. The table records no clinical significance for this variant.

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Reference-table entries

JDP2Not classified

Variant type: missense_variant
Chromosome / position: 14:75904660
HGVS: NM_001135049.1,c.70A>G,p.Thr24Ala
Allele change: Missense_T13A

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.