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Variant (rsID / SNP)

rs2286469

ZNF598

rs2286469 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF598. Location: chromosome 16, position 2,049,640. The table records no clinical significance for this variant.

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Reference-table entries

ZNF598Not classified
Variant type
missense_variant
Chromosome / position
16:2049640
HGVS
NM_178167.4,c.1910T>C,p.Met637Thr
Allele change
Missense_M637T

Public references

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