Variant (rsID / SNP)

rs794728092

rs794728092 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DSG2. Location: chromosome 18, position 29,102,123. Clinical significance in the table: Pathogenic.

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Reference-table entries

DSG2Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: Deletion
Chromosome / position: 18:29102123
Cytoband: 18q12.1
HGVS: NM_001943.5(DSG2):c.601_605del (p.Val201fs)

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.