Variant (rsID / SNP)

rs140816500

rs140816500 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GRXCR2. Location: chromosome 5, position 145,252,378. Clinical significance in the table: Uncertain significance.

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Reference-table entries

GRXCR2Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 5:145252378
Cytoband: 5q32
HGVS: NM_001080516.2(GRXCR2):c.154A>G (p.Ser52Gly)
Allele change: Missense_S52G

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.