Variant (rsID / SNP)

rs2074888

rs2074888 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TCF3. Location: chromosome 19, position 1,615,796. The table records no clinical significance for this variant.

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Reference-table entries

TCF3Not classified

Variant type: missense_variant
Chromosome / position: 19:1615796
HGVS: NM_003200.5,c.1475C>T,p.Ala492Val
Allele change: Missense_A492V

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.