Variant (rsID / SNP)

rs28368004

rs28368004 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ECE1. Location: chromosome 1, position 21,571,475. Clinical significance in the table: Benign.

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Reference-table entries

ECE1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:21571475
Cytoband: 1p36.12
HGVS: NM_001397.3(ECE1):c.1278+7C>T
Allele change: Silent

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.