Variant (rsID / SNP)

rs11648894

rs11648894 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RNF166. Location: chromosome 16, position 88,766,359. The table records no clinical significance for this variant.

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Reference-table entries

RNF166Not classified

Variant type: intron_variant
Chromosome / position: 16:88766359
HGVS: NM_178841.4,c.313-219G>A
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.