Variant (rsID / SNP)

rs1536690

rs1536690 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF169. Location: chromosome 9, position 97,055,310. The table records no clinical significance for this variant.

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Reference-table entries

ZNF169Not classified

Variant type: missense_variant
Chromosome / position: 9:97055310
HGVS: NM_003448.3,c.215C>T,p.Pro72Leu
Allele change: Missense_P72L

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.