Variant (rsID / SNP)

rs12949528

rs12949528 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LINC00469. Location: chromosome 17, position 71,747,473. The table records no clinical significance for this variant.

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Reference-table entries

LINC00469Not classified

Variant type: intron_variant
Chromosome / position: 17:71747473
HGVS: NR_027146.1,n.321-836T>C
Allele change: Missense_H168R

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.