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Variant (rsID / SNP)

rs1024323

GRK4

rs1024323 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GRK4. Location: chromosome 4, position 3,006,043. The table records no clinical significance for this variant.

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Reference-table entries

GRK4Not classified
Variant type
missense_variant
Chromosome / position
4:3006043
HGVS
NM_182982.3,c.425C>T,p.Ala142Val
Allele change
Silent

Associated conditions / phenotypes

Pre-Eclampsia|Hypercholesterolemia, Familial, 1|Hypercholesterolemia, Familial, 3

Public references

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