Variant (rsID / SNP)

rs62453384

rs62453384 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABCB5. Location: chromosome 7, position 20,762,646. The table records no clinical significance for this variant.

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Reference-table entries

ABCB5Not classified

Variant type: missense_variant
Chromosome / position: 7:20762646
HGVS: NM_001163941.2,c.2429G>T,p.Gly810Val
Allele change: Missense_G810V

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.