Variant (rsID / SNP)

rs4862650

rs4862650 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FAM149A. Location: chromosome 4, position 187,074,833. The table records no clinical significance for this variant.

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Reference-table entries

FAM149ANot classified

Variant type: missense_variant
Chromosome / position: 4:187074833
HGVS: NM_001395294.1,c.994A>G,p.Lys332Glu
Allele change: Missense_K41E

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.