Variant (rsID / SNP)

rs61755050

rs61755050 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NR1H4. Location: chromosome 12, position 100,926,308. Clinical significance in the table: Likely benign.

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Reference-table entries

NR1H4Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 12:100926308
Cytoband: 12q23.1
HGVS: NM_001206979.2(NR1H4):c.518T>C (p.Met173Thr)
Allele change: Missense_M173T

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.