Variant (rsID / SNP)

rs3739238

rs3739238 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC45A4. Location: chromosome 8, position 142,222,445. The table records no clinical significance for this variant.

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Reference-table entries

SLC45A4Not classified

Variant type: missense_variant
Chromosome / position: 8:142222445
HGVS: NM_001286646.2,c.2152A>G,p.Asn718Asp
Allele change: Missense_N667D

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.