Variant (rsID / SNP)

rs1051624

rs1051624 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDH17. Location: chromosome 8, position 95,143,172. The table records no clinical significance for this variant.

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Reference-table entries

CDH17Not classified

Variant type: missense_variant
Chromosome / position: 8:95143172
HGVS: NM_001144663.2,c.2216A>C,p.Glu739Ala
Allele change: Missense_E739A

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.