Variant (rsID / SNP)

rs377767355

rs377767355 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SMAD4. Location: chromosome 18, position 48,593,397. Clinical significance in the table: Uncertain significance.

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Reference-table entries

SMAD4Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 18:48593397
Cytoband: 18q21.2
HGVS: NM_005359.6(SMAD4):c.1148T>A (p.Ile383Lys)
Allele change: Missense_I383K

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.