Variant (rsID / SNP)

rs9894429

rs9894429 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NPLOC4. Location: chromosome 17, position 79,596,811. The table records no clinical significance for this variant.

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Reference-table entries

NPLOC4Not classified

Variant type: synonymous_variant
Chromosome / position: 17:79596811
HGVS: NM_001369698.1,c.36G>A,p.Pro12Pro
Allele change: Synonymous_P12P

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.