Variant (rsID / SNP)

rs16959856

rs16959856 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DSG4. Location: chromosome 18, position 28,968,371. Clinical significance in the table: Benign.

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Reference-table entries

DSG4Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 18:28968371
Cytoband: 18q12.1
HGVS: NM_177986.5(DSG4):c.258G>A (p.Arg86=)
Allele change: Silent

Associated conditions / phenotypes

Hypotrichosis 6

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.