rs372944937
- Uncertain significance
Your Genotype
Sign InDescription
This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868].
In silico analysis supports that this missense variant does not alter protein structure/function; Has not been previously published as pathogenic or benign to our knowledge
Reference Allele
A
Alternative Allele
C
Chromosome
20
Location
10405335
Variant Type
SNP
Genes
ClinVar
Name
NM_170784.3(MKKS):c.1625T>G (p.Leu542Trp)
Allele
C
Clinical Significance
Uncertain significance