Variant (rsID / SNP)

rs2241586

rs2241586 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF610. Location: chromosome 19, position 52,869,022. The table records no clinical significance for this variant.

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Reference-table entries

ZNF610Not classified

Variant type: missense_variant
Chromosome / position: 19:52869022
HGVS: NM_001161425.2,c.391G>T,p.Ala131Ser
Allele change: Missense_A131S

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.