Variant (rsID / SNP)

rs1197669

rs1197669 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to JMJD7-PLA2G4B. Location: chromosome 15, position 42,138,456. The table records no clinical significance for this variant.

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Reference-table entries

JMJD7-PLA2G4BNot classified

Variant type: synonymous_variant
Chromosome / position: 15:42138456
HGVS: NM_005090.4,c.2349G>A,p.Arg783Arg
Allele change: Synonymous_R783R

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.