Variant (rsID / SNP)

rs7198494

rs7198494 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C16ORF46, C16orf46. Location: chromosome 16, position 81,095,091. The table records no clinical significance for this variant.

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Reference-table entries

C16ORF46Not classified

Variant type: missense_variant
Chromosome / position: 16:81095091
HGVS: NM_152337.3,c.863T>C,p.Ile288Thr
Allele change: Missense_I288T

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.