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Variant (rsID / SNP)

rs1699233

SHLD1

rs1699233 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SHLD1. Location: chromosome 20, position 5,843,812. The table records no clinical significance for this variant.

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Reference-table entries

SHLD1Not classified
Variant type
synonymous_variant
Chromosome / position
20:5843812
HGVS
NM_001303477.2,c.321T>C,p.Gly107Gly
Allele change
Synonymous_G75G

Public references

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