Variant (rsID / SNP)

rs550818

rs550818 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TP53I13, GIT1. Location: chromosome 17, position 27,901,975. The table records no clinical significance for this variant.

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Reference-table entries

TP53I13Not classified

Variant type: downstream_gene_variant
Chromosome / position: 17:27901975
HGVS: NM_138349.4,c.*2033A>G
Allele change: Silent

Associated conditions / phenotypes

Attention Deficit-Hyperactivity Disorder

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.