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Variant (rsID / SNP)

rs3749147

GPN1

rs3749147 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GPN1. Location: chromosome 2, position 27,851,918. The table records no clinical significance for this variant.

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Reference-table entries

GPN1Not classified
Variant type
5_prime_UTR_variant
Chromosome / position
2:27851918
HGVS
NM_007266.4,c.-8G>A
Allele change
Silent

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.