Variant (rsID / SNP)

rs61732039

rs61732039 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABCB5. Location: chromosome 7, position 20,687,604. The table records no clinical significance for this variant.

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Reference-table entries

ABCB5Not classified

Variant type: missense_variant
Chromosome / position: 7:20687604
HGVS: NM_001163941.2,c.1109A>G,p.Asp370Gly
Allele change: Missense_D370G

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.