Variant (rsID / SNP)

rs1055207

rs1055207 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TEX48. Location: chromosome 9, position 117,428,960. The table records no clinical significance for this variant.

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Reference-table entries

TEX48Not classified

Variant type: missense_variant
Chromosome / position: 9:117428960
HGVS: NM_001199233.2,c.326A>G,p.His109Arg
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.