Variant (rsID / SNP)

rs1128349

rs1128349 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNAJC30. Location: chromosome 7, position 73,097,654. The table records no clinical significance for this variant.

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Reference-table entries

DNAJC30Not classified

Variant type: missense_variant
Chromosome / position: 7:73097654
HGVS: NM_032317.3,c.100G>A,p.Gly34Arg
Allele change: Missense_G34R

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.