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Variant (rsID / SNP)

rs4888262

RFWD3

rs4888262 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RFWD3. Location: chromosome 16, position 74,670,458. The table records no clinical significance for this variant.

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Reference-table entries

RFWD3Not classified
Variant type
synonymous_variant
Chromosome / position
16:74670458
HGVS
NM_001370534.1,c.1212G>A,p.Thr404Thr
Allele change
Synonymous_T404T

Public references

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