Variant (rsID / SNP)

rs4465613

rs4465613 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MIR11401, SLC7A5. Location: chromosome 16, position 87,892,271. The table records no clinical significance for this variant.

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Reference-table entries

MIR11401Not classified

Variant type: downstream_gene_variant
Chromosome / position: 16:87892271
HGVS: NR_162122.1,n.*4701T>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.