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Variant (rsID / SNP)

rs584855

ANKRD60

rs584855 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ANKRD60. Location: chromosome 20, position 56,793,706. The table records no clinical significance for this variant.

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Reference-table entries

ANKRD60Not classified
Variant type
missense_variant
Chromosome / position
20:56793706
HGVS
NM_001304369.2,c.883C>T,p.Arg295Cys
Allele change
Missense_R295C

Public references

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