Variant (rsID / SNP)

rs10413455

rs10413455 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF134. Location: chromosome 19, position 58,131,623. The table records no clinical significance for this variant.

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Reference-table entries

ZNF134Not classified

Variant type: missense_variant
Chromosome / position: 19:58131623
HGVS: NM_003435.5,c.136G>A,p.Ala46Thr
Allele change: Missense_A46T

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.