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Variant (rsID / SNP)

rs1136697

HLA-A

rs1136697 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HLA-A. Location: chromosome 6, position 29,911,069. The table records no clinical significance for this variant.

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Reference-table entries

HLA-ANot classified
Variant type
missense_variant
Chromosome / position
6:29911069
HGVS
NM_002116.8,c.368A>T,p.Tyr123Phe
Allele change
Missense_Y123S

Associated conditions / phenotypes

Nasopharyngeal Carcinoma

Public references

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