Variant (rsID / SNP)

rs10410631

rs10410631 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF550. Location: chromosome 19, position 58,058,739. The table records no clinical significance for this variant.

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Reference-table entries

ZNF550Not classified

Variant type: synonymous_variant
Chromosome / position: 19:58058739
HGVS: NM_001277090.2,c.873A>G,p.Gln291Gln
Allele change: Synonymous_Q291Q

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.