Variant (rsID / SNP)

rs4467099

rs4467099 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LOC400499. Location: chromosome 16, position 11,542,894. The table records no clinical significance for this variant.

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Reference-table entries

LOC400499Not classified

Variant type: missense_variant
Chromosome / position: 16:11542894
HGVS: NM_001370704.1,c.4327G>A,p.Ala1443Thr

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.