Variant (rsID / SNP)

rs2073924

rs2073924 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GBGT1. Location: chromosome 9, position 136,037,742. The table records no clinical significance for this variant.

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Reference-table entries

GBGT1Not classified

Variant type: missense_variant
Chromosome / position: 9:136037742
HGVS: NM_021996.6,c.58C>T,p.Leu20Phe
Allele change: Missense_L20F

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.