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Variant (rsID / SNP)

rs1139652

DNAJA3

rs1139652 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNAJA3. Location: chromosome 16, position 4,476,089. The table records no clinical significance for this variant.

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Reference-table entries

DNAJA3Not classified
Variant type
missense_variant
Chromosome / position
16:4476089
HGVS
NM_001286516.2,c.97T>C,p.Tyr33His
Allele change
Missense_Y33H

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.