Variant (rsID / SNP)

rs734028

rs734028 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PLEKHH1. Location: chromosome 14, position 68,053,802. The table records no clinical significance for this variant.

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Reference-table entries

PLEKHH1Not classified

Variant type: synonymous_variant
Chromosome / position: 14:68053802
HGVS: NM_020715.3,c.3945T>C,p.Ala1315Ala
Allele change: Synonymous_A1315A

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.