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Variant (rsID / SNP)

rs8058922

RFWD3

rs8058922 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RFWD3. Location: chromosome 16, position 74,695,079. The table records no clinical significance for this variant.

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Reference-table entries

RFWD3Not classified
Variant type
missense_variant
Chromosome / position
16:74695079
HGVS
NM_001370534.1,c.269C>A,p.Thr90Asn
Allele change
Missense_T90N

Public references

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