Variant (rsID / SNP)

rs144166918

rs144166918 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CNTLN. Location: chromosome 9, position 17,394,994. The table records no clinical significance for this variant.

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Reference-table entries

CNTLNNot classified

Variant type: missense_variant
Chromosome / position: 9:17394994
HGVS: NM_017738.4,c.2542C>T,p.His848Tyr
Allele change: Missense_H848Y

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.