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Variant (rsID / SNP)

rs881118

CHGB

rs881118 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CHGB. Location: chromosome 20, position 5,903,388. The table records no clinical significance for this variant.

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Reference-table entries

CHGBNot classified
Variant type
missense_variant
Chromosome / position
20:5903388
HGVS
NM_001819.3,c.598A>C,p.Asn200His
Allele change
Missense_N200H

Public references

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