Variant (rsID / SNP)

rs2306933

rs2306933 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FAM189A1. Location: chromosome 15, position 29,421,054. The table records no clinical significance for this variant.

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Reference-table entries

FAM189A1Not classified

Variant type: missense_variant
Chromosome / position: 15:29421054
HGVS: NM_015307.2,c.941G>A,p.Gly314Asp
Allele change: Missense_G314D

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.