Variant (rsID / SNP)

rs201754946

rs201754946 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KRT4. Location: chromosome 12, position 53,203,235. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

KRT4Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 12:53203235
Cytoband: 12q13.13
HGVS: NM_002272.4(KRT4):c.766G>A (p.Val256Met)
Allele change: Missense_V256M

Associated conditions / phenotypes

White sponge nevus 1

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.