Variant (rsID / SNP)

rs1407390

rs1407390 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SHOC1. Location: chromosome 9, position 114,464,487. The table records no clinical significance for this variant.

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Reference-table entries

SHOC1Not classified

Variant type: missense_variant
Chromosome / position: 9:114464487
HGVS: NM_001378211.1,c.2987A>G,p.Tyr996Cys
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.