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Variant (rsID / SNP)

rs17611866

ZNF75A

rs17611866 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF75A. Location: chromosome 16, position 3,367,229. The table records no clinical significance for this variant.

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Reference-table entries

ZNF75ANot classified
Variant type
missense_variant
Chromosome / position
16:3367229
HGVS
NM_001302109.2,c.974T>C,p.Val325Ala
Allele change
Silent

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.