Variant (rsID / SNP)

rs1902767

rs1902767 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LINC00592, LINC02874. Location: chromosome 12, position 52,602,013. The table records no clinical significance for this variant.

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Reference-table entries

LINC00592Not classified

Variant type: upstream_gene_variant
Chromosome / position: 12:52602013
HGVS: NR_027358.2,n.-2701C>T
Allele change: Missense_R38Q

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.