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Variant (rsID / SNP)

rs11693860

FAM228B

rs11693860 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FAM228B. Location: chromosome 2, position 24,369,674. The table records no clinical significance for this variant.

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Reference-table entries

FAM228BNot classified
Variant type
synonymous_variant
Chromosome / position
2:24369674
HGVS
NM_001145710.2,c.498C>T,p.Asn166Asn
Allele change
Silent

Public references

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