Variant (rsID / SNP)

rs916362

rs916362 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MIR3667HG. Location: chromosome 22, position 50,017,234. The table records no clinical significance for this variant.

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Reference-table entries

MIR3667HGNot classified

Variant type: intron_variant
Chromosome / position: 22:50017234
HGVS: NR_110523.2,n.115+33819T>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.