Variant (rsID / SNP)

rs140172891

rs140172891 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SMO. Location: chromosome 7, position 128,852,242. The table records no clinical significance for this variant.

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Reference-table entries

SMONot classified

Variant type: single nucleotide variant
Chromosome / position: 7:128852242
Cytoband: 7q32.1
HGVS: NM_005631.5(SMO):c.2314C>T (p.Arg772Cys)
Allele change: Missense_R772C

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.