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Variant (rsID / SNP)

rs41271862

DST

rs41271862 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DST. Location: chromosome 6, position 56,373,536. The table records no clinical significance for this variant.

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Reference-table entries

DSTNot classified
Variant type
missense_variant
Chromosome / position
6:56373536
HGVS
NM_001374736.1,c.19030G>A,p.Asp6344Asn
Allele change
Missense_D4087N

Public references

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