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Variant (rsID / SNP)

rs6022903

BCAS1

rs6022903 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BCAS1. Location: chromosome 20, position 52,612,549. The table records no clinical significance for this variant.

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Reference-table entries

BCAS1Not classified
Variant type
missense_variant
Chromosome / position
20:52612549
HGVS
NM_001366298.2,c.764G>A,p.Gly255Glu
Allele change
Missense_G255E

Public references

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