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Variant (rsID / SNP)

rs35898523

GBGT1

rs35898523 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GBGT1. Location: chromosome 9, position 136,029,645. The table records no clinical significance for this variant.

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Reference-table entries

GBGT1Not classified
Variant type
stop_gained
Chromosome / position
9:136029645
HGVS
NM_021996.6,c.363C>A,p.Tyr121*
Allele change
Nonsense_Y104X

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.