Variant (rsID / SNP)

rs13409104

rs13409104 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ALLC. Location: chromosome 2, position 3,718,692. The table records no clinical significance for this variant.

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Reference-table entries

ALLCNot classified

Variant type: 5_prime_UTR_premature_start_codon_gain_variant
Chromosome / position: 2:3718692
HGVS: NM_018436.4,c.-56C>T
Allele change: Silent

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.