Variant (rsID / SNP)

rs6843860

rs6843860 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NDST4. Location: chromosome 4, position 115,749,005. The table records no clinical significance for this variant.

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Reference-table entries

NDST4Not classified

Variant type: synonymous_variant
Chromosome / position: 4:115749005
HGVS: NM_022569.3,c.2586G>A,p.Ser862Ser
Allele change: Synonymous_S862S

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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