Variant (rsID / SNP)

rs35221142

rs35221142 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RFT1. Location: chromosome 3, position 53,155,720. Clinical significance in the table: Benign.

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Reference-table entries

RFT1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 3:53155720
Cytoband: 3p21.1
HGVS: NM_052859.4(RFT1):c.553G>A (p.Ala185Thr)
Allele change: Missense_A185T

Associated conditions / phenotypes

RFT1-congenital disorder of glycosylation

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.