Variant (rsID / SNP)

rs6438869

rs6438869 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HEG1. Location: chromosome 3, position 124,728,626. The table records no clinical significance for this variant.

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Reference-table entries

HEG1Not classified

Variant type: missense_variant
Chromosome / position: 3:124728626
HGVS: NM_020733.2,c.3116T>C,p.Met1039Thr
Allele change: Missense_M1039T

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.