Variant (rsID / SNP)
rs1056141
rs1056141 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FERMT1. Location: chromosome 20, position 6,096,632. Clinical significance in the table: Benign.
Reference-table entries
FERMT1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 20:6096632
- Cytoband
- 20p12.3
- HGVS
- NM_017671.5(FERMT1):c.211C>T (p.Leu71=)
- Allele change
- Synonymous_L71L
Associated conditions / phenotypes
Kindler syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.