Variant (rsID / SNP)

rs12631989

rs12631989 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IHO1. Location: chromosome 3, position 49,273,996. The table records no clinical significance for this variant.

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Reference-table entries

IHO1Not classified

Variant type: synonymous_variant
Chromosome / position: 3:49273996
HGVS: NM_001135197.2,c.72C>T,p.Ser24Ser
Allele change: Synonymous_S24S

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.