Variant (rsID / SNP)

rs186443359

rs186443359 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TTI2. Location: chromosome 8, position 33,369,551. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

TTI2Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 8:33369551
Cytoband: 8p12
HGVS: NM_001102401.4(TTI2):c.581G>C (p.Gly194Ala)
Allele change: Missense_G194A

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.