Variant (rsID / SNP)

rs10818759

rs10818759 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RC3H2. Location: chromosome 9, position 125,652,757. The table records no clinical significance for this variant.

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Reference-table entries

RC3H2Not classified

Variant type: synonymous_variant
Chromosome / position: 9:125652757
HGVS: NM_001100588.3,c.417C>T,p.Asn139Asn
Allele change: Synonymous_N139N

Associated conditions / phenotypes

Synonymous_N139N

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.