Variant (rsID / SNP)

rs7539980

rs7539980 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GSTM5. Location: chromosome 1, position 110,257,947. The table records no clinical significance for this variant.

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Reference-table entries

GSTM5Not classified

Variant type: intron_variant
Chromosome / position: 1:110257947
HGVS: NM_000851.4,c.567+85A>C
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.