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Variant (rsID / SNP)

rs34433105

ZNF169

rs34433105 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF169. Location: chromosome 9, position 97,062,295. The table records no clinical significance for this variant.

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Reference-table entries

ZNF169Not classified
Variant type
missense_variant
Chromosome / position
9:97062295
HGVS
NM_003448.3,c.458C>T,p.Ser153Leu
Allele change
Missense_S152L

Public references

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