rs34282046
- Benign/Likely benign
Your Genotype
Sign InDescription
Variant identified in a genome or exome case(s) and assessed due to predicted null impact of the variant or pathogenic assertions in the literature or databases. Disclaimer: This variant has not undergone full assessment. The following are preliminary notes: Frequency
Reference Allele
G
Alternative Allele
C
Chromosome
19
Location
19194090
Variant Type
SNP
Genes
MEF2BNB-MEF2B
MEF2BNB
Phenotypes
ClinVar
Name
NM_003721.4(RFXANK):c.144G>C (p.Glu48Asp)
Allele
C
Clinical Significance
Benign/Likely benign