Variant (rsID / SNP)

rs9873604

rs9873604 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZKSCAN7. Location: chromosome 3, position 44,612,050. The table records no clinical significance for this variant.

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Reference-table entries

ZKSCAN7Not classified

Variant type: missense_variant
Chromosome / position: 3:44612050
HGVS: NM_001288590.2,c.1448C>T,p.Thr483Ile
Allele change: Missense_T332I

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.