Variant (rsID / SNP)

rs151187899

rs151187899 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GSR. Location: chromosome 8, position 30,550,502. Clinical significance in the table: Uncertain significance.

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Reference-table entries

GSRUncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 8:30550502
Cytoband: 8p12
HGVS: NM_000637.5(GSR):c.866T>C (p.Val289Ala)
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.