Variant (rsID / SNP)
rs3743582
rs3743582 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LITAF. Location: chromosome 16, position 11,650,325. Clinical significance in the table: Benign.
Reference-table entries
LITAFBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- intron_variant
- Chromosome / position
- 16:11650325
- HGVS
- NM_001136472.2,c.220+42C>T
- Allele change
- Silent
Associated conditions / phenotypes
Charcot-Marie-Tooth Disease, Demyelinating, Type 1c
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.