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Variant (rsID / SNP)

rs6591182

EHBP1L1

rs6591182 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EHBP1L1. Location: chromosome 11, position 65,349,756. The table records no clinical significance for this variant.

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Reference-table entries

EHBP1L1Not classified
Variant type
missense_variant
Chromosome / position
11:65349756
HGVS
NM_001099409.3,c.1613T>G,p.Val538Gly
Allele change
Silent

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.