Variant (rsID / SNP)

rs231228

rs231228 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ARHGAP33. Location: chromosome 19, position 36,268,771. The table records no clinical significance for this variant.

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Reference-table entries

ARHGAP33Not classified

Variant type: synonymous_variant
Chromosome / position: 19:36268771
HGVS: NM_001366178.1,c.150C>T,p.Ala50Ala
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.