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Variant (rsID / SNP)

rs2276924

FAM149A

rs2276924 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FAM149A. Location: chromosome 4, position 187,078,785. The table records no clinical significance for this variant.

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Reference-table entries

FAM149ANot classified
Variant type
missense_variant
Chromosome / position
4:187078785
HGVS
NM_001395294.1,c.1514A>G,p.His505Arg
Allele change
Missense_H214R

Public references

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