Variant (rsID / SNP)

rs5748623

rs5748623 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to XKR3. Location: chromosome 22, position 17,265,124. The table records no clinical significance for this variant.

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Reference-table entries

XKR3Not classified

Variant type: missense_variant
Chromosome / position: 22:17265124
HGVS: NM_001318251.3,c.765T>G,p.Phe255Leu
Allele change: Missense_F255L

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.