Variant (rsID / SNP)

rs2307424

rs2307424 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NR1I3. Location: chromosome 1, position 161,202,605. Clinical significance in the table: Benign.

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Reference-table entries

NR1I3Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:161202605
Cytoband: 1q23.3
HGVS: NM_005122.5(NR1I3):c.540C>T (p.Pro180=)
Allele change: Synonymous_P180P

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.