Variant (rsID / SNP)

rs2526374

rs2526374 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RNF43. Location: chromosome 17, position 56,435,885. Clinical significance in the table: Benign.

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Reference-table entries

RNF43Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 17:56435885
Cytoband: 17q22
HGVS: NM_017763.6(RNF43):c.1252C>A (p.Leu418Met)
Allele change: Missense_L418M

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.