Variant (rsID / SNP)

rs2818384

rs2818384 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to JAKMIP3. Location: chromosome 10, position 133,961,494. The table records no clinical significance for this variant.

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Reference-table entries

JAKMIP3Not classified

Variant type: synonymous_variant
Chromosome / position: 10:133961494
HGVS: NM_001323086.2,c.1788C>T,p.His596His
Allele change: Synonymous_H522H

Associated conditions / phenotypes

Synonymous_H596H

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.