Variant (rsID / SNP)

rs1105223

rs1105223 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CRB2. Location: chromosome 9, position 126,128,211. The table records no clinical significance for this variant.

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Reference-table entries

CRB2Not classified

Variant type: missense_variant
Chromosome / position: 9:126128211
HGVS: NM_173689.7,c.434T>C,p.Met145Thr
Allele change: Missense_M145T

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.