Variant (rsID / SNP)
rs2232387
rs2232387 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KRT75. Location: chromosome 12, position 52,827,608. Clinical significance in the table: risk factor.
Reference-table entries
KRT75Risk factor
- Clinical significance (as recorded)
- risk factor
- Variant type
- single nucleotide variant
- Chromosome / position
- 12:52827608
- Cytoband
- 12q13.13
- HGVS
- NM_004693.3(KRT75):c.481G>A (p.Ala161Thr)
- Allele change
- Missense_A161T
Associated conditions / phenotypes
Pseudofolliculitis barbae
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.