Variant (rsID / SNP)
rs56163822
rs56163822 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NR1H4. Location: chromosome 12, position 100,887,101. Clinical significance in the table: Benign.
Reference-table entries
NR1H4Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 12:100887101
- Cytoband
- 12q23.1
- HGVS
- NM_001206979.2(NR1H4):c.-1G>T
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.