Variant (rsID / SNP)

rs741164

rs741164 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C16ORF89, C16orf89. Location: chromosome 16, position 5,106,184. The table records no clinical significance for this variant.

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Reference-table entries

C16ORF89Not classified

Variant type: synonymous_variant
Chromosome / position: 16:5106184
HGVS: NM_152459.5,c.633G>A,p.Gly211Gly
Allele change: Synonymous_G211G

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.