Variant (rsID / SNP)

rs33928105

rs33928105 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GRK7. Location: chromosome 3, position 141,535,608. The table records no clinical significance for this variant.

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Reference-table entries

GRK7Not classified

Variant type: missense_variant
Chromosome / position: 3:141535608
HGVS: NM_139209.3,c.1378C>A,p.Pro460Thr
Allele change: Missense_P460T

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.