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Variant (rsID / SNP)

rs10221698

KIAA2012

rs10221698 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KIAA2012. Location: chromosome 2, position 202,939,654. The table records no clinical significance for this variant.

Reference-table entries

KIAA2012Not classified
Variant type
missense_variant
Chromosome / position
2:202939654
HGVS
NM_001277372.4,c.125T>C,p.Val42Ala
Allele change
Missense_V42A

Public references

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