Variant (rsID / SNP)

rs112218090

rs112218090 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IFT27. Location: chromosome 22, position 37,158,995. Clinical significance in the table: Benign.

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Reference-table entries

IFT27Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 22:37158995
Cytoband: 22q12.3
HGVS: NM_001177701.3(IFT27):c.415C>T (p.Arg139Trp)
Allele change: Silent

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.