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Variant (rsID / SNP)

rs698775

PREPL

rs698775 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PREPL. Location: chromosome 2, position 44,588,941. The table records no clinical significance for this variant.

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Reference-table entries

PREPLNot classified
Variant type
5_prime_UTR_variant
Chromosome / position
2:44588941
HGVS
NM_001171603.1,c.-314C>T
Allele change
Silent

Public references

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