Variant (rsID / SNP)

rs7927138

rs7927138 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OVCH2. Location: chromosome 11, position 7,727,886. The table records no clinical significance for this variant.

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Reference-table entries

OVCH2Not classified

Variant type: missense_variant
Chromosome / position: 11:7727886
HGVS: NM_198185.7,c.56G>A,p.Arg19Gln
Allele change: Missense_R19Q

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.