Variant (rsID / SNP)

rs62441157

rs62441157 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNRC18. Location: chromosome 7, position 5,347,746. The table records no clinical significance for this variant.

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Reference-table entries

TNRC18Not classified

Variant type: synonymous_variant
Chromosome / position: 7:5347746
HGVS: NM_001080495.3,c.8898G>A,p.Val2966Val
Allele change: Synonymous_V2966V

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.