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Variant (rsID / SNP)

rs1042337

HLA-DMB

rs1042337 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HLA-DMB. Location: chromosome 6, position 32,904,981. The table records no clinical significance for this variant.

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Reference-table entries

HLA-DMBNot classified
Variant type
missense_variant
Chromosome / position
6:32904981
HGVS
NM_002118.5,c.590C>T,p.Thr197Ile
Allele change
Missense_T197I

Public references

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