Variant (rsID / SNP)

rs6973420

rs6973420 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CALD1. Location: chromosome 7, position 134,618,710. The table records no clinical significance for this variant.

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Reference-table entries

CALD1Not classified

Variant type: missense_variant
Chromosome / position: 7:134618710
HGVS: NM_033138.4,c.1190A>G,p.His397Arg
Allele change: Silent

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.