Variant (rsID / SNP)

rs1007298

rs1007298 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RGL4, GUSBP11. Location: chromosome 22, position 24,038,847. The table records no clinical significance for this variant.

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Reference-table entries

RGL4Not classified

Variant type: missense_variant
Chromosome / position: 22:24038847
HGVS: NM_001329424.3,c.1133T>C,p.Val378Ala
Allele change: Silent

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.