Variant (rsID / SNP)

rs61746143

rs61746143 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SMO. Location: chromosome 7, position 128,843,396. Clinical significance in the table: Benign.

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Reference-table entries

SMOBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 7:128843396
Cytoband: 7q32.1
HGVS: NM_005631.5(SMO):c.503G>A (p.Arg168His)
Allele change: Missense_R168H

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.