Variant (rsID / SNP)

rs11657054

rs11657054 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GGT6. Location: chromosome 17, position 4,463,023. The table records no clinical significance for this variant.

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Reference-table entries

GGT6Not classified

Variant type: missense_variant
Chromosome / position: 17:4463023
HGVS: NM_001288702.2,c.173C>T,p.Ala58Val
Allele change: Missense_A58V

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.