Variant (rsID / SNP)

rs237422

rs237422 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SHLD1. Location: chromosome 20, position 5,753,579. The table records no clinical significance for this variant.

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Reference-table entries

SHLD1Not classified

Variant type: missense_variant
Chromosome / position: 20:5753579
HGVS: NM_001303477.2,c.68C>T,p.Ala23Val
Allele change: Silent

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.