Variant (rsID / SNP)
rs3206707
rs3206707 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HNRNPA1. Location: chromosome 12, position 54,678,089. Clinical significance in the table: Likely benign.
Reference-table entries
HNRNPA1Likely benign
- Clinical significance (as recorded)
- Likely benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 12:54678089
- Cytoband
- 12q13.13
- HGVS
- NM_031157.4(HNRNPA1):c.1111A>G (p.Arg371Gly)
- Allele change
- Missense_R371G
Associated conditions / phenotypes
Relapsing remitting multiple sclerosis
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.