Variant (rsID / SNP)

rs6477845

rs6477845 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SHOC1. Location: chromosome 9, position 114,462,322. The table records no clinical significance for this variant.

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Reference-table entries

SHOC1Not classified

Variant type: missense_variant
Chromosome / position: 9:114462322
HGVS: NM_001378211.1,c.3095T>C,p.Leu1032Pro
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.