Variant (rsID / SNP)

rs6983214

rs6983214 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C8ORF44, C8orf44. Location: chromosome 8, position 67,590,460. The table records no clinical significance for this variant.

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Reference-table entries

C8ORF44Not classified

Variant type: intron_variant
Chromosome / position: 8:67590460
HGVS: NR_161216.1,n.419+271C>T
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.