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Variant (rsID / SNP)

rs3998860

TET1

rs3998860 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TET1. Location: chromosome 10, position 70,405,855. The table records no clinical significance for this variant.

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Reference-table entries

TET1Not classified
Variant type
missense_variant
Chromosome / position
10:70405855
HGVS
NM_030625.3,c.3369A>G,p.Ile1123Met
Allele change
Missense_I1123M

Associated conditions / phenotypes

Non-Alcoholic Fatty Liver Disease|Liver Disease|Fatty Liver Disease

Public references

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