Variant (rsID / SNP)

rs3762672

rs3762672 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNAJC13. Location: chromosome 3, position 132,218,623. The table records no clinical significance for this variant.

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Reference-table entries

DNAJC13Not classified

Variant type: missense_variant
Chromosome / position: 3:132218623
HGVS: NM_001329126.2,c.4402G>T,p.Ala1468Ser
Allele change: Missense_A1468S

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.