Variant (rsID / SNP)

rs2960306

rs2960306 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GRK4. Location: chromosome 4, position 2,990,499. The table records no clinical significance for this variant.

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Reference-table entries

GRK4Not classified

Variant type: missense_variant
Chromosome / position: 4:2990499
HGVS: NM_182982.3,c.194G>T,p.Arg65Leu
Allele change: Silent

Associated conditions / phenotypes

Hypercholesterolemia, Familial, 1|Hypercholesterolemia, Familial, 3

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.