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Variant (rsID / SNP)

rs1032141

TIAM2

rs1032141 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TIAM2. Location: chromosome 6, position 155,485,554. The table records no clinical significance for this variant.

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Reference-table entries

TIAM2Not classified
Variant type
synonymous_variant
Chromosome / position
6:155485554
HGVS
NM_001384546.1,c.2034G>A,p.Gln678Gln
Allele change
Synonymous_Q678Q

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.