Variant (rsID / SNP)

rs34161743

rs34161743 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NR1I3. Location: chromosome 1, position 161,203,078. 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: 1:161203078
Cytoband: 1q23.3
HGVS: NM_005122.5(NR1I3):c.289C>T (p.Arg97Trp)
Allele change: Missense_R97W

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.