Variant (rsID / SNP)

rs6823734

rs6823734 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NAAA. Location: chromosome 4, position 76,836,137. The table records no clinical significance for this variant.

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Reference-table entries

NAAANot classified

Variant type: missense_variant&splice_region_variant
Chromosome / position: 4:76836137
HGVS: NM_014435.4,c.1000T>C,p.Phe334Leu
Allele change: Silent

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.