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Variant (rsID / SNP)

rs3796028

TNS1

rs3796028 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNS1. Location: chromosome 2, position 218,695,102. The table records no clinical significance for this variant.

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Reference-table entries

TNS1Not classified
Variant type
missense_variant
Chromosome / position
2:218695102
HGVS
NM_001308022.2,c.3010C>T,p.Arg1004Trp
Allele change
Silent

Associated conditions / phenotypes

Body Mass Index Quantitative Trait Locus 1

Public references

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