Variant (rsID / SNP)

rs55923022

rs55923022 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IQSEC3. Location: chromosome 12, position 248,155. The table records no clinical significance for this variant.

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Reference-table entries

IQSEC3Not classified

Variant type: synonymous_variant
Chromosome / position: 12:248155
HGVS: NM_001170738.2,c.1626C>T,p.Ala542Ala
Allele change: Synonymous_A542A

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.