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Variant (rsID / SNP)

rs11119314

CAMK1G

rs11119314 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CAMK1G. Location: chromosome 1, position 209,782,343. The table records no clinical significance for this variant.

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Reference-table entries

CAMK1GNot classified
Variant type
synonymous_variant
Chromosome / position
1:209782343
HGVS
NM_020439.3,c.654A>G,p.Pro218Pro
Allele change
Synonymous_P218P

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.