Variant (rsID / SNP)

rs2011404

rs2011404 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UGT1A4, UGT1A10. Location: chromosome 2, position 234,627,937. The table records no clinical significance for this variant.

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Reference-table entries

UGT1A4Not classified

Variant type: synonymous_variant
Chromosome / position: 2:234627937
HGVS: NM_007120.3,c.471T>C,p.Cys157Cys
Allele change: Silent

Associated conditions / phenotypes

Mycobacterium Tuberculosis 1|Liver Disease|Lung Cancer Susceptibility 1|Type 2 Diabetes Mellitus|Diabetes Mellitus

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.