Variant (rsID / SNP)

rs168726

rs168726 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZFP62. Location: chromosome 5, position 180,276,402. The table records no clinical significance for this variant.

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Reference-table entries

ZFP62Not classified

Variant type: missense_variant
Chromosome / position: 5:180276402
HGVS: NM_001172638.2,c.2093G>A,p.Arg698Lys
Allele change: Synonymous_Q720Q

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.