Variant (rsID / SNP)

rs2741098

rs2741098 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to XKR5. Location: chromosome 8, position 6,690,276. The table records no clinical significance for this variant.

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Reference-table entries

XKR5Not classified

Variant type: missense_variant
Chromosome / position: 8:6690276
HGVS: NM_207411.5,c.205A>G,p.Met69Val
Allele change: Missense_M69V

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.