Variant (rsID / SNP)

rs1053593

rs1053593 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HMGXB4. Location: chromosome 22, position 35,660,875. The table records no clinical significance for this variant.

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Reference-table entries

HMGXB4Not classified

Variant type: missense_variant
Chromosome / position: 22:35660875
HGVS: NM_001003681.3,c.494G>T,p.Gly165Val
Allele change: Silent

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.