Variant (rsID / SNP)

rs72681869

rs72681869 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SOS2. Location: chromosome 14, position 50,655,357. Clinical significance in the table: Uncertain significance.

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Reference-table entries

SOS2Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 14:50655357
Cytoband: 14q21.3
HGVS: NM_006939.4(SOS2):c.572C>T (p.Pro191Leu)
Allele change: Missense_P191R

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.