Variant (rsID / SNP)

rs11555693

rs11555693 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IFT74. Location: chromosome 9, position 26,978,259. The table records no clinical significance for this variant.

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Reference-table entries

IFT74Not classified

Variant type: missense_variant&splice_region_variant
Chromosome / position: 9:26978259
HGVS: NM_001099222.3,c.254A>G,p.Lys85Arg
Allele change: Missense_K85R

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.