Variant (rsID / SNP)

rs4797625

rs4797625 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ANKRD62. Location: chromosome 18, position 12,130,394. The table records no clinical significance for this variant.

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Reference-table entries

ANKRD62Not classified

Variant type: downstream_gene_variant
Chromosome / position: 18:12130394
HGVS: NM_001277333.2,c.*2456G>A

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.