Variant (rsID / SNP)

rs61743204

rs61743204 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SON. Location: chromosome 21, position 34,926,043. The table records no clinical significance for this variant.

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Reference-table entries

SONNot classified

Variant type: missense_variant
Chromosome / position: 21:34926043
HGVS: NM_138927.4,c.4506G>A,p.Met1502Ile
Allele change: Missense_M1502I

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.