Variant (rsID / SNP)

rs55765823

rs55765823 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SMAD5. Location: chromosome 5, position 135,513,085. The table records no clinical significance for this variant.

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Reference-table entries

SMAD5Not classified

Variant type: frameshift_variant&splice_region_variant
Chromosome / position: 5:135513085
HGVS: NM_001001419.3,c.1313-1_1313insC,p.Asn438fs

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.