rs1138958
- Benign
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
C
G
Chromosome
9
Location
113278969
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001244926.2(PRPF4):c.230A>G (p.His77Arg)
Allele
G
Clinical Significance
Benign