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Variant (rsID / SNP)

rs17235766

CD101

rs17235766 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CD101. Location: chromosome 1, position 117,560,036. The table records no clinical significance for this variant.

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Reference-table entries

CD101Not classified
Variant type
missense_variant
Chromosome / position
1:117560036
HGVS
NM_001256106.3,c.1553G>A,p.Arg518Gln
Allele change
Missense_R456Q

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.