Variant (rsID / SNP)

rs4925042

rs4925042 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC47A2. Location: chromosome 17, position 19,608,773. The table records no clinical significance for this variant.

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Reference-table entries

SLC47A2Not classified

Variant type: synonymous_variant
Chromosome / position: 17:19608773
HGVS: NM_152908.5,c.993C>T,p.Tyr331Tyr
Allele change: Silent

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.