Variant (rsID / SNP)

rs2217652

rs2217652 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF559-ZNF177, ZNF177. Location: chromosome 19, position 9,490,814. The table records no clinical significance for this variant.

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Reference-table entries

ZNF559-ZNF177Not classified

Variant type: missense_variant&splice_region_variant
Chromosome / position: 19:9490814
HGVS: NM_001384659.1,c.335C>T,p.Thr112Met
Allele change: Missense_T112M

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.