Variant (rsID / SNP)

rs1749409

rs1749409 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RIT1. Location: chromosome 1, position 155,870,416. Clinical significance in the table: Benign.

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Reference-table entries

RIT1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:155870416
Cytoband: 1q22
HGVS: NM_006912.6(RIT1):c.430-7C>T
Allele change: Silent

Associated conditions / phenotypes

Noonan syndrome 8

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.