Variant (rsID / SNP)

rs7975356

rs7975356 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OVCH1. Location: chromosome 12, position 29,630,081. The table records no clinical significance for this variant.

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Reference-table entries

OVCH1Not classified

Variant type: missense_variant
Chromosome / position: 12:29630081
HGVS: NM_001353179.2,c.1436C>T,p.Thr479Ile
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.