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Variant (rsID / SNP)

rs11127

GNLY

rs11127 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GNLY. Location: chromosome 2, position 85,924,729. The table records no clinical significance for this variant.

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Reference-table entries

GNLYNot classified
Variant type
missense_variant
Chromosome / position
2:85924729
HGVS
NM_001302758.2,c.437C>T,p.Thr146Ile
Allele change
Missense_T119I

Associated conditions / phenotypes

Hepatitis B|Hepatitis|Mycobacterium Tuberculosis 1|Liver Disease

Public references

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