Variant (rsID / SNP)

rs139471643

rs139471643 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SPZ1. Location: chromosome 5, position 79,616,278. The table records no clinical significance for this variant.

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Reference-table entries

SPZ1Not classified

Variant type: missense_variant
Chromosome / position: 5:79616278
HGVS: NM_032567.4,c.244A>G,p.Asn82Asp
Allele change: Missense_N82D

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.