Variant (rsID / SNP)

rs10812505

rs10812505 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IFT74. Location: chromosome 9, position 26,978,170. The table records no clinical significance for this variant.

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Reference-table entries

IFT74Not classified

Variant type: missense_variant
Chromosome / position: 9:26978170
HGVS: NM_001099222.3,c.165A>G,p.Ile55Met
Allele change: Missense_I55M

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.