Variant (rsID / SNP)

rs4141499

rs4141499 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KBTBD12. Location: chromosome 3, position 127,641,968. The table records no clinical significance for this variant.

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Reference-table entries

KBTBD12Not classified

Variant type: missense_variant
Chromosome / position: 3:127641968
HGVS: NM_001370224.1,c.64C>A,p.Gln22Lys
Allele change: Missense_Q22K

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.