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Variant (rsID / SNP)

rs236153

CHGB

rs236153 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CHGB. Location: chromosome 20, position 5,903,894. The table records no clinical significance for this variant.

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Reference-table entries

CHGBNot classified
Variant type
synonymous_variant
Chromosome / position
20:5903894
HGVS
NM_001819.3,c.1104A>G,p.Glu368Glu
Allele change
Synonymous_E368E

Public references

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