Variant (rsID / SNP)

rs12601097

rs12601097 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ODF4. Location: chromosome 17, position 8,243,661. The table records no clinical significance for this variant.

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Reference-table entries

ODF4Not classified

Variant type: missense_variant
Chromosome / position: 17:8243661
HGVS: NM_153007.5,c.292G>A,p.Val98Met
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.