Variant (rsID / SNP)

rs628778

rs628778 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RNF113B, FARP1. Location: chromosome 13, position 98,829,176. The table records no clinical significance for this variant.

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Reference-table entries

RNF113BNot classified

Variant type: synonymous_variant
Chromosome / position: 13:98829176
HGVS: NM_178861.5,c.315A>G,p.Pro105Pro
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.