Variant (rsID / SNP)

rs3796619

rs3796619 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RNF212. Location: chromosome 4, position 1,095,281. Clinical significance in the table: association.

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Reference-table entries

RNF212Association

Clinical significance (as recorded): association
Variant type: single nucleotide variant
Chromosome / position: 4:1095281
Cytoband: 4p16.3
HGVS: NM_001131034.4(RNF212):c.172-4654T>C
Allele change: Silent

Associated conditions / phenotypes

Recombination rate quantitative trait locus 1

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.