Variant (rsID / SNP)

rs5919015

rs5919015 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HEPH. The table records no clinical significance for this variant.

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Reference-table entries

HEPHNot classified

Variant type: 5_prime_UTR_variant
HGVS: NM_138737.6,c.-47T>C
Allele change: Missense_V39A

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.